Pharmaceutical Composition for Treating STK11-Mutation Cancer Using Cardiac Glycosides

Abstract

The present invention relates to a pharmaceutical composition for treating STK11-mutation cancer, containing, as an active ingredient, a material inhibiting a sodium-potassium transport function of Na.sup.+K.sup.+ ATPase (ATP1A1); an anticancer drug containing the composition as an active ingredient; and a method for screening STK11-mutation cancer therapeutic agent. It was first established that, of cancer cells in which various gene mutations are confirmed, an STK11-mutation cancer cell line, which is confirmed at high frequency, was treated with cardiac glycosides as a material inhibiting a sodium-potassium transport function of Na.sup.+K.sup.+ ATPase (ATP1A1), to significantly inhibit the growth of cancer cells. Therefore, the material inhibiting a sodium-potassium transport function of Na.sup.+K.sup.+ ATPase (ATP1A1) can be a target for treating SK11-mutation-derived cancer.

Claims

1. A method for treating cancers harboring STK11 (serine/threonine kinase 11 mutation, comprising: administering an effective amount of a pharmaceutical composition containing a material for inhibiting a sodium-potassium transport function of Na.sup.+K.sup.+ ATPase (sodium/potassium-transporting ATPase subunit alpha-1; ATP1A1) as an active ingredient to a subject in need thereof for treating serine/threonine kinase 11 (STK11)-mutation cancer.

2. The method of claim 1, wherein the cancer is selected from the group consisting of prostate cancer, breast cancer, colon cancer, melanoma, and lung cancer.

3. The method claim 1, wherein the Na.sup.+K.sup.+ ATPase has an amino acid sequence set forth in SEQ ID NO: 1.

4. The method of claim 1, wherein the material for inhibiting a sodium-potassium transport function of Na.sup.+K.sup.+ ATPase comprises a cardiac glycoside, or a material specifically binding to Na.sup.+K.sup.+ ATPase.

5. The method of claim 4, wherein the material specifically binding to Na.sup.+K.sup.+ ATPase is selected from the group consisting of siRNA, shRNA, and an antisense oligonucleotide of a Na.sup.+K.sup.+ ATPase gene.

6. The method of claim 4, wherein the cardiac glycoside is selected from the group consisting of digoxin, ouabain, and digitoxin.

7. (canceled)

8. (canceled)

9. A method for diagnosising cancers harboring STK11 (serine/threonine kinase 11) mutation, comprising the following steps: (1) collecting a biological sample from a patient to separate cells; (2) bringing a material for inhibiting a sodium-potassium transport function of Na.sup.+K.sup.+ ATPase (sodium/potassium-transporting ATPase subunit alpha-1; ATP1A1) into contact with the cells; and (3) determining that the cells have a high probability of becoming STK11-mutant cancer when the growth of the cells is inhibited, compared to an untreated group.

10. The method of claim 9, wherein the biological sample in Step (1) is selected from the group consisting of blood, skin cells, mucosal cells, urine, and hair.

11. The method of claim 9, wherein the cancer is selected from the group consisting of prostate cancer, breast cancer, colon cancer, melanoma, and lung cancer.

12. A method for screening a therapeutic agent for cancers harboring STK11 (serine/threonine kinase 11) mutation, comprising the following steps: a) bringing a material for inhibiting a sodium-potassium transport function of Na.sup.+K.sup.+ ATPase (sodium/potassium-transporting ATPase subunit alpha-1; ATP1A1) into contact with STK11-mutant cancer cells and STK11-wild-type cancer cells; b) comparing growth rates of the STK11-mutant cancer cells and the STK11-wild-type cancer cells after the contact; and c) selecting a material which inhibits the growth of the STK11-mutant cancer cells as a therapeutic agent for STK11-mutant cancer.

13. The method of claim 12, wherein the cancer is selected from the group consisting of prostate cancer, breast cancer, colon cancer, melanoma, and lung cancer.

14. (canceled)

15. (canceled)

16. (canceled)

Description

DESCRIPTION OF DRAWINGS

[0037] FIG. 1 shows structural formulas of cardiac glycosides proposed to be effective against STK11 mutant cancer according to one exemplary embodiment of the present invention.

[0038] FIG. 2 shows results of determining STK11 mutation patterns in non-small cell lung cancer (NSCLC). FIG. 2A shows a genetic variation pattern of seven major mutations in patients suffering from lung adenocarcinoma which is one of NSCLC subtypes of the non-small cell lung cancer (NSCLC) and accounts for the highest proportion of non-small cell lung cancer (NSCLC). FIG. 2B shows STK11 mutation frequencies (%) according to the cancer progression of lung adenocarcinoma.

[0039] FIG. 3A is a heat map obtained by hierarchically clustering of the three cardiac glycosides shown in FIG. 1 in 60 cancer cell lines, and FIG. 3B shows results of measuring relative drug effects (AUC values at logGI.sub.50) of therapeutic agents for non-small cell lung cancer (NSCLC) used in the prior art and the cardiac glycosides in STK11 mutant cell lines, compared to those in cell lines in which STK11 is normally expressed.

[0040] FIG. 4 shows logGI.sub.50 waterfall plots for enrichments of the compounds (digoxin, digitoxin and ouabain) having the respective structures shown in FIG. 1 in STK11 mutant cell lines, compared to those in the wild-type cell line (the plots shown in FIGS. 4A, 4B and 4C to correspond to the compounds, respectively).

[0041] FIG. 5A is a graph of the results of determining inhibition of the cell growth in 8 lung cancer cell lines when a STK11-mutant lung cancer cell line and an STK11-wild-type lung cancer cell line are treated with a varying concentration of digoxin, digitoxin and ouabain (72 hours), and FIG. 5B is a graph of the results of determining inhibition of the cell growth after wild-type STK11 is expressed in the STK11-mutant lung cancer cell line.

[0042] FIG. 6 is a graph of the results of determining effects of digoxin, digitoxin and ouabain on relative inhibition of the cell growth in an STK11 mutant cell line (A549), compared to a cell line (A549-STK11) in which STK11 is normally expressed: the inhibition of the cell growth is determined at the days 3, 7 and 14 (TiterBlue) after the STK11 mutant cell line and the cell line in which STK11 is restored are treated with digoxin, digitoxin and ouabain for a long time.

[0043] FIGS. 7A and 7B show results of evaluating cell viability in lung cancer cell lines after lung cancer cell lines are treated with ATP1A1 siRNA (72 hours): FIG. 7A shows TiterBlue results of evaluating cell viability after an STK11-mutant lung cancer cell line and an STK11-wild-type lung cancer cell line are treated with ATP1A1 siRNA, and FIG. 7B shows TiterBlue results of evaluating the cell viability after wild-type STK11 is expressed in the STK11-mutant lung cancer cell line.

[0044] FIG. 8 is a graph of the results of comparing the inhibition of the growth of cells obtained by knocking down both ATP1A1 and STK11 (72 hours) in two lung cancer cell lines having wild-type STK11.

[0045] FIG. 9 shows results of determining inhibitory effects on specific cell migration and cell division in STK11-mutant lung cancer cell lines when the STK11-mutant lung cancer cell lines are treated with cardiac glycosides; FIG. 9A shows results of cell migration, and FIG. 9B shows results of cell division.

[0046] FIG. 10 shows results of determining preclinical effects of cardiac glycosides in STK11-mutant lung cancer: FIG. 10A shows results of determining the growth of a tumor in an animal model into which an A549 cell line is incorporated, FIG. 10B shows results of determining the growth of a tumor in an animal model into which a cell line in which STK11 is restored into the wild type is incorporated, FIGS. 10C, 10D, and 10E are graphs and an image of determining a relative decrease in tumor growth in the animal model into which the STK11-mutant cells are incorporated, compared to that in the animal model into which the cell line in which STK11 is normally expressed is incorporated, when both the cell lines are treated with the cardiac glycosides at a concentration of 60 ng/ind. (3 g/kg) and 180 ng/ind. (9 g/kg), respectively.

BEST MODE

[0047] Hereinafter, the present invention will be described in further detail, as follows.

[0048] The present invention is characterized in that it provides a pharmaceutical composition for treating STK11-mutant cancer, which includes, as an active ingredient, a material for inhibiting a sodium-potassium transport function of Na.sup.+K.sup.+ ATPase (ATP1A1).

[0049] In the present invention, it has been found by analyzing the characteristics of mutation-specific cancer, which provide new understanding of cancer treatment using various sets of data due to an increase in usefulness of data on human cell lines and tissues that the growth of cancer cells is inhibited when STK11-mutant cancer cells are treated with a material for inhibiting a sodium-potassium transport function of ATP1A1 compared to the wild-type cancer cell line. Therefore, the present invention has been completed based on this fact.

[0050] ATP1A1 signaling pathways currently known in the art include activation of mTOR, promotion of a decrease in ATP1A1 activity by AICAR-induced AMPK activation, activation of mitogen-activated protein kinase (MAPK), activation of mitochondrial reactive oxygen species (ROS), activation of phospholipase and inositol triphosphate (IP3) receptors (IP3R), etc.

[0051] In the present invention, a material for inhibiting a sodium-potassium transport function of ATP1A1 in STK11-mutant-type cancer, particularly a material specifically binding to ATP1A1 to inhibit an intracellular potassium transport function, is confirmed to be a target for treating STK11-mutation-derived cancer.

[0052] Also, according to one exemplary embodiment of the present invention, it was directly confirmed that, when cancer cells are treated with cardiac glycosides as a material for inhibiting a sodium-potassium transport function of ATP1A1, an inhibitory effect on the growth of cancer cells is significantly produced in STK11 mutant-type cancer cells, compared to the wild-type cancer cells (cancer cells having no mutations in a STK11 protein).

[0053] In addition, according to one exemplary embodiment of the present invention, it was experimentally confirmed that, when cancer cells are treated with ATP1A1 siRNA as the material for inhibiting a sodium-potassium transport function of ATP1A1, the ATP1A1 knockdown inhibits the cell growth in STK11-mutated cancer cell lines.

[0054] Based on the results, it can be seen that the material for inhibiting a sodium-potassium transport function of ATP1A1 may be used to treat cancers harboring STK11 mutation. This also provides a possible route for therapeutic applications to control the progression of cancer (especially STK11-mutated cancer). Also, in the present invention, it was confirmed that the STK11 knockdown has an effect similar to ATP1A1. The ATP1A1 knockdown induces a selective decrease in the cell growth in STK11 mutant cell lines. This indicates that the expression of ATP1A1 is important for cell growth when normal STK11 signaling disappears. In addition, most ATP1A1 inhibitors have superior cell growth inhibitory activities in STK11 mutant cancer cell lines, compared to the STK11 wild-type cancer cell line.

[0055] To sum up, the results of the present invention provide a therapeutic potential for STK11 mutant-type cancer using a novel therapeutic method using the material for inhibiting a sodium-potassium transport function of ATP1A1. Therefore, an approach of the present invention may provide an effective clue to a novel effective therapeutic method.

[0056] Therefore, based on the experimental results of the present invention, the present invention may provide a pharmaceutical composition for treating STK11-mutant cancer, which includes, as an active ingredient, a material for inhibiting a sodium-potassium transport function of Na.sup.+K.sup.+ ATPase (ATP1A1), and may also provide a pharmaceutical composition for diagnosing STK11-mutant cancer, which includes, as an active ingredient, a material for inhibiting a sodium-potassium transport function of Na.sup.+K.sup.+ ATPase (ATP1A1).

[0057] STK11 mutations are found a wide range of cancers including prostate cancer, breast cancer, colon cancer, lymphoma, melanoma, lung cancer, etc. In this regard, the present inventors have elucidated that a material for inhibiting a sodium-potassium transport function of ATP1A1, particularly a material serving to inhibit an intracellular potassium transport function of ATP1A1 by specifically binding to an ATP1A1 pump to competitively or non-competitively inhibit binding of potassium to ATP1A1, specifically inhibits the growth of STK11-mutant cancer. Most preferably, it has been found that, when the material for inhibiting a sodium-potassium transport function of ATP1A1 is used in lung cancers in which STK11 mutations are detected at higher frequency than that of other cancers, the material for inhibiting a sodium-potassium transport function of ATP1A1 may be effectively applied to treat STK11-mutation lung cancer among the cancers.

[0058] An ATP1A1 protein of the present invention may have an amino acid sequence set forth in SEQ ID NO: 1, which is derived from a human, but the present invention is not limited thereto. In this case, the ATP1A1 protein may include a protein having an amino acid sequence having a homology of 70% or more, preferably 80% or more, more preferably 90% or more, and most preferably 95% with the amino acid sequence.

[0059] It has been confirmed that the inhibition of ATP1A1 in a series of lung cancer cell lines causes a significant decrease in cell growth in STK11-mutant cancer cell lines other than the wild-type cancer cell line, and it has been found that ATP1A1 plays an important role in cell viability or growth in the STK11-mutant cancer cell lines. These results suggest that ATP1A1 participates in progression of STK11-mutant cancer, indicating that the growth of STK11-mutant cancer cells is inhibited when a function of an ATP1A1 pump is suppressed, which makes it possible to treat STK11-mutant cancer.

[0060] In the present invention, the material for inhibiting a sodium-potassium transport function of ATP1A1 includes cardiac glycosides, or a material specifically binding to ATP1A1. Here, the material specifically binding to ATP1A1 may be selected from the group consisting of siRNA, shRNA, and an antisense oligonucleotide of an ATP1A1 gene, but the present invention is not limited thereto.

[0061] The antisense oligonucleotide refers to an oligomer that is hybridized with a target sequence in RNA through Watson-Crick base pairing to form an oligomeric heterodimer between mRNA and RNA in the target sequence. The antisense oligonucleotide has complete or similar sequence complementarity to the target sequence, may interfere with or inhibit translation of mRNA, and may inhibit expression of a target gene by changing a procedure of processing mRNA to generate splicing variants. According to one exemplary embodiment of the present invention, the antisense oligonucleotide inhibiting expression of the ATP1A1 protein may be an oligomer having a sequence complementary to mRNA of a gene coding for the ATP1A1 protein having the amino acid sequence set forth in SEQ ID NO: 1.

[0062] siRNA refers to a double-stranded RNA which has a length of approximately 20 nucleotides and may mediate RNA interference or gene silencing, and the shRNA refers to an RNA which has a short hair-pin structure and is positioned between loops in which each of sense and antisense sequences of an siRNA target sequence consists of 5 to 9 bases. siRNA or shRNA is known to specifically bind to target mRNA having a complementary sequence to induce RNA interference (RNAi) through mRNA cleavage of a target gene. According to one exemplary embodiment of the present invention, siRNA or shRNA that inhibits the expression of the ATP1A1 protein having an amino acid sequence set forth in SEQ ID NO: 1 may have a sequence complementary to mRNA of a gene coding for ATP1A1.

[0063] A method of preparing siRNA includes a method of chemically synthesizing siRNA, or a method of synthesizing siRNA using in vitro transcription, but the present invention is not limited thereto. Also, shRNA is used to overcome the drawbacks of the siRNA, such as high synthesis cost, short duration of an RNA interference effect due to low transfection efficiency, etc., and may be introduced into cells and expressed from a promoter of RNA polymerase III using adenoviral, lentiviral, and plasmid expression vector systems. shRNA is known to be converted into siRNA having an accurate structure by an siRNA processing enzyme (Dicer or RNase III) present in the cells in order to induce silencing of a target gene.

[0064] Also, the material for inhibiting a sodium-potassium transport function of ATP1A1 may be a monoclonal or polyclonal antibody that specifically binds to ATP1A1 to specifically inhibit a pumping function. The antibody may specifically bind to an ATP1A1 pump to effectively inhibit an intracellular potassium transport function of ATP1A1. The antibody specifically binding to ATP1A1 may be prepared using methods known to those skilled in the related art, or commercially available antibodies may be purchased and used. Also, the antibody binding to ATP1A1 to inhibit a potassium pumping function includes an intact full-length antibody having two heavy chains and two light chains, and a functional fragment thereof. The functional fragment of the antibody refers to a fragment having at least an antigen-binding function, and includes Fab, F(ab), F(ab)2, and Fv, etc.

[0065] In addition, the material for inhibiting a sodium-potassium transport function of ATP1A1 may be known cardiac glycosides. The known cardiac glycosides may include a compound, a natural substance, an extract, and a bioactive substance, all of which are known to inhibit a pumping function of ATP1A1, for example, digoxin, ouabain, or digitoxin, etc., but the present invention is not limited thereto.

[0066] Digoxin binds to a site on an extracellular side of an a-subunit of ATP1A1 (Na.sup.+K.sup.+ ATPase). Ouabain is a compound which is isolated from a plant and widely used in in vitro studies by scientists to specifically block a sodium pump. As the cardiac glycoside, digitoxin has a structure and effect similar to digoxin, but the effect of digitoxin lasts for a longer time than digoxin. The above-described digoxin, ouabain, and digitoxin are compounds known to directly and specifically inhibit ATP1A1.

[0067] For studies of these currently known compounds, digoxin has been widely used to treat various heart conditions. Digoxin has been proposed to have a beneficial effect on the heart, and reduce the risk of certain carcinoma, but digoxin is just proposed to have an effect of reducing the risk of cancer when the drug is used at a therapeutic concentration.

[0068] Considering ouabain, there are known studies showing that ouabain as a cardiac glycoside is a potent therapeutic target against lung cancer, and delays invasion of lung cancer cells, known studies examining that an effect of ouabain on cytotoxicity and a signaling pathway of PC-3 cells in order to determine the potential of the cardiac glycoside to treat androgen-dependent prostate cancers, etc.

[0069] Considering digitoxin, there is a known study showing that pharmacological research is performed on digitoxin and analogues thereof to develop a potent chemotherapeutic drug with a focus on the cytotoxicity of the digitoxin and analogues for cancer cells, and a conventional mechanism for an effect of digitoxin on ATP1A1 is established as a new mechanism.

[0070] However, there are no studies showing that such cardiac glycosides specifically inhibit the cell growth in STK11-mutant cancer.

[0071] The pharmaceutical composition according to the present invention may include the active ingredient at 0.0001 to 50% by weight, based on the total weight of the composition, but the present invention is not limited thereto. The composition according to the present invention may further include a pharmaceutically acceptable carrier for the purpose of use as the pharmaceutical composition. The pharmaceutically acceptable carrier is generally used to prepare a formulation, and includes lactose, dextrose, sucrose, sorbitol, mannitol, starch, gum acacia, calcium phosphate, alginate, gelatin, calcium silicate, microcrystalline cellulose, polyvinyl pyrrolidone, cellulose, water, syrup, methylcellulose, methyl hydroxybenzoate, propyl hydroxybenzoate, talc, magnesium stearate, and mineral oil, but the present invention is not limited thereto. In addition to the above-described components, the pharmaceutical composition of the present invention may further include a lubricant, a wetting agent, a sweetening agent, a flavoring agent, an emulsifying agent, a suspending agent, a preservative, etc. Proper pharmaceutically acceptable carriers and formulations are generally known in the related art.

[0072] The pharmaceutical composition of the present invention may be orally or parenterally administered. For parenteral administration, the pharmaceutical composition may be administered by intravenous injection, local injection, intraventricular injection, intrathecal injection, subcutaneus injection, intraperitoneal injection, transdermal administration, etc.

[0073] A proper dose of the pharmaceutical composition of the present invention varies, depending on factors including a method of formulation, a mode of administration, age, body weight, sex, and morbidity of a patient, diet, an administration time, a route of administration, an excretion rate, and sensitivity to a reaction. In general, an effective dose of the composition suitable for desired treatment and prevention may be readily determined and prescribed by skilled practitioners. Preferably, the pharmaceutical composition according to the present invention may be administered at a dose of 0.001 to 100 mg/kg/day.

[0074] The pharmaceutical composition of the present invention may be prepared into formulations in the form of a unit dose using a pharmaceutically acceptable carrier or excipient, or may be prepared into multi-dose containers according to methods which may be easily performed by those skilled in the art to which the present invention belongs. In this case, the formulation may be in the form of a solution in oil or an aqueous medium, a suspension or an emulsion, or may also be in the form of an extract, a powder, a granule, a tablet, or a capsule, and may further include a dispersing agent or a stabilizing agent.

[0075] From the foregoing, the pharmaceutical composition of the present invention may be provided as an anticancer drug for treating STK11 mutant cancer.

[0076] Also, the present invention may provide a method for treating STK11 mutant cancer, which includes administering the pharmaceutical composition or the anticancer drug to a subject in need of treatment of STK11 mutant cancer. Here, the subject may include a primate including a human, livestock (cattle, a horse, a sheep, a chicken, a pig, a dog, and a rabbit), etc., but the present invention is not limited thereto.

[0077] In addition, the present invention may provide a method for diagnosing STK11-mutant cancer, which includes treating cells with the material for inhibiting a sodium-potassium transport function of ATP1A1 and determining that the cells have a high probability of becoming STK11-mutant cancer when the cell growth is inhibited, compared to the normal control.

[0078] In addition, the present invention may provide a method for screening a therapeutic agent for STK11-mutant cancer, which includes bringing a material for inhibiting a sodium-potassium transport function of ATP1A1 into contact with STK11-mutant cancer cells and STK11-wild-type cancer cells in vitro, comparing growth rates of the STK11-mutant cancer cells and the STK11-wild-type cancer cells after the contact, and selecting a material which specifically inhibits the growth of the STK11-mutant cancer cells as a therapeutic agent for STK11-mutant cancer.

[0079] In the present invention, it was confirmed that the material for inhibiting a sodium-potassium transport function of ATP1A1 inhibits the cell growth in the STK11-mutant cancer cells, compared to the STK11-wild-type cancer cells. Also, it was revealed that the growth of the STK11-mutant cancer cells is inhibited when ATP1A1 is knocked down in the STK11-mutant cancer cells.

[0080] Therefore, the material specifically binding to ATP1A1 to inhibit a function of an ATP1A1 pump may inhibit the growth of the STK11-mutant cancer cells to show a cancer treatment effect. In this case, the cancer may be selected from the group consisting of prostate cancer, breast cancer, colon cancer, melanoma, and lung cancer.

[0081] Also, in the screening method according to the present invention, the bringing of the material for inhibiting a sodium-potassium transport function of ATP1A1 (a test material) into contact with the STK11-mutant cancer cells and the STK11-wild-type cancer cells may be performed by transfecting, transforming or injecting the test material. Here, the contact with the test material may be performed in a medium in which the growth of the cells may be constantly maintained.

[0082] In the screening method, the comparing of the growth rates of the STK11-mutant cancer cells and the STK11-wild-type cancer cells may be performed by counting the cells. Here, the cell counting may be carried out with the naked eye, or carried out using software after images are photographed, but the present invention is not limited thereto.

[0083] In the screening method, when the cell growth rate of the STK11-mutant cancer cells is inhibited compared to the cell growth rate of the wild-type cancer cells after the cancer cells are treated with the test material, the test material may be selected as a material that may inhibit a function of an ATP1A1 pump, and thus may be used to treat STK11-mutant cancer.

Mode for Invention

[0084] Hereinafter, the present invention will be described in further detail with reference to examples thereof. However, it should be understood that the following examples provided herein are merely intended to more specifically describe the present invention, and are not intended to limit the scope of the present invention.

EXAMPLE 1: HIERARCHICAL CLUSTERING OF STK11 GENOTYPE-SPECIFIC COMPOUNDS

[0085] To identify sensitivity patterns of the genotype-specific compounds, a subset of the compounds was selected using a GI.sub.50 profile pattern on a CLEA map.

[0086] First of all, a logGI.sub.50 value of 8 (that is, GI50=0.01 M) was chosen as a bipartite cutoff used to determine to which cell lines a compound was sensitive on a NCI60 panel. In this case, the compound was sensitive when the value is greater than 8, and was not sensitive when the value is less than 8.

[0087] Next, an enrichment score (an AUC value) was used to select the genotype-specific compounds in a CLEA assay.

[0088] An AUC value >80 and a P value <0.01 were used as cutoff values used to determine that a compound had significant sensitivity to certain genotypes. In this example, compounds showing strong potency (that is, a logGI.sub.50 value of 8) to at least one cell line on the NCI60 panel were included.

[0089] As a result, a total of three non-overlapping compounds satisfying the above filtering requirements were compiled. Hierarchical clustering of these selected compounds was carried out on a category of STK11 genotypes. The results are shown in FIG. 3A. In this example, three main groups of compounds showing uniform sensitivity based on the mutant genotypes were identified. Such a cluster of compounds were sensitive to genetic mutations in an STK11 gene. These results provide a direct clue to understanding a mechanism of action (MOA) among the various compounds having similar applications.

[0090] Also, FIG. 3B shows that the cardiac glycosides have higher sensitivity to STK11 mutant-type lung cancer, compared to the therapeutic agents for lung cancer (non-small cell lung cancer; NSCLC) previously approved by the FDA.

EXAMPLE 2: STK11 GENOTYPE-DEPENDENT SENSITIVITY OF COMPOUNDS

[0091] Three representative compounds (ouabain, digoxin, and digitoxin) were selected from the clusters shown in FIG. 3A to further analyze a genotype-specific cellular reaction.

[0092] From the genetic variation pattern shown in FIG. 2A, it was revealed that STK11 (LKB1) mutation is mutually exclusive from other major lung cancer mutations in tissues from a non-small cell lung cancer (NSCLC) patient. Therefore, there was a need for the development of anti-cancer drugs specific to a group of STK11 mutant-type lung cancer patients. From the graph showing the variation frequencies of STK11 mutations according to the progression stage of cancer shown in FIG. 2B, it was confirmed that the frequencies of STK11 mutations increased according to the progression of lung cancer. However, although clinical trials of anti-cancer drugs had been actively conducted on mutations of the genes such as ALK, BRAF, and EGFR in lung cancer, there were no reports on the development of an anticancer drug that targets STK11-mutations with optionally high frequency. Therefore, a need for the development of a pharmaceutical composition having a therapeutic effect specific to STK11-mutant lung cancer is proposed.

[0093] Also, STK11 codes for a serine-threonine kinase that directly phosphorylates a central metabolic sensor AMPK to be activated. AMPK regulates lipid, cholesterol, and glucose metabolisms in specialized metabolic tissues such as liver, muscle, and fatty tissue. An STK11 protein participates in two biologically important pathways of causing cancer. First, STK11 aids in maintaining polarized epithelial cells. Second, STK11 activates AMPK controlling the balance of cellular energy. This insight into the functions of STK11 alludes to a proposition that the STK11 may be a target for novel therapeutic strategy through regulation of AMPK activity.

[0094] In this example, it was revealed that the ouabain, digoxin, and digitoxin belonged to a cluster associated with the STK11 mutations, and that these compounds showed relatively high sensitivity in 6 cell lines with STK11 mutation potential, as shown in FIG. 3A.

[0095] The 6 cell lines with STK11 mutation potential are listed in Table 1 below.

TABLE-US-00001 TABLE 1 MOLT-4 Leukemia CDKN2A; NOTCH1; NRAS; PTEN; TP53; STK11; A549 Lung CDKN2A; KRAS; STK11 NCI-H460 Lung CDKN2A; KRAS; PIK3CA; STK11; c-MYC- Amp NCI-H23 Lung KRAS; STK11; TP53; PTEN; CTNNB1 SK-MEL-5 Melanoma BRAF; CDKN2A; STK11 DU-145 Prostate CDKN2A; MLH1; RB1; STK11; TP53

[0096] Meanwhile, FIG. 4 shows logGI.sub.50 waterfall plots for enrichments of the compounds (digoxin, digitoxin, and ouabain) having the respective structures shown in FIG. 1 in STK11 mutant cell lines, compared to those in the wild-type cell line (the plots shown in FIGS. 4A, 4B and 4C to correspond to the compounds, respectively).

[0097] From the results shown in FIGS. 3 and 4, it was revealed that all the three cardiac glycoside drugs clearly showed the STK11-specific sensitivity.

[0098] As a result, it can be defined that the cardiac glycosides drugs had STK11 mutation-dependent activity.

EXAMPLE 3: ANALYSIS OF INHIBITORY EFFECT SPECIFIC STK11-MUTANT LUNG CANCERS ON CELL GROWTH BY TREATMENT OF CARDIAC GLYCOSIDES

[0099] (1) Cell Line Culture

[0100] NCI-60 lung cancer cell lines (NCI-H460, A549, NCI-H322M, and NCI-H226) were obtained from the U.S. National Cancer Institute (NCI DTP). All cells were grown in an RPMI medium (GIBCO) supplemented with 10% FBS (GIBCO) and penicillin/streptavidin (GIBCO), and kept at 37 C. in a humidified atmosphere of 5% CO.sub.2.

[0101] (2) Analysis of Cell Vviability

[0102] A total of three cardiac glycosides (chemicals) having the structures shown in FIG. 1 were screened in a lung cancer cell line. Digoxin, ouabain, and digitoxin were all purchased from Sigma Aldrich.

[0103] The cells were seeded in 96-well plates at a density of 2,000, 1,000, and 200 cells per well, and cultured for 3, 7, and 14 days, respectively. After 24 hours of seeding, the cells were treated with a chemical diluted with digitoxin and ouabain at working concentrations of 0.05 M and 0.02 M, respectively. The cells were again cultured for 72 hours (3 days), 7 days, and 14 days, and then the cell viability was measured using a CellTiter-Blue assay kit.

[0104] Four STK11-mutant lung cancer cell lines (A549, H460, H1993, and H1395) and four STK11-wild-type lung cancer cell lines (H226, H322M, H82, and H524) were treated with a varying concentration of digoxin, digitoxin, and ouabain as the cardiac glycosides for 72 hours to check whether the cell growth was inhibited. The respective results are shown in FIG. 5A.

[0105] From the results of FIG. 5A, it can be seen that the STK11-mutant lung cancer cell lines had higher sensitivity to the respective compounds, compared to the STK11-wild-type lung cancer cell lines.

[0106] Therefore, it was confirmed that the cell growth was inhibited when the lung cancer cell lines were treated with digoxin, digitoxin, and ouabain in the 96-well plate. In this case, each of a STK11-mutant cell line (A549) and a cell line (A549-STK11) in which STK11 was restored into the wild type were used as the lung cancer cell line.

[0107] FIG. 5B is a graph of the results of determining inhibition of the cell growth after the cell lines are treated with each of digoxin, digitoxin, and ouabain (TiterBlue). It can be seen that the cell line in which STK11 was restored was resistant to the treated compounds, compared to the STK11-mutant cell line.

[0108] Also, FIG. 6 shows a difference in viability between the STK11-mutant cell line (A549) and the cell line (A549-STK11) in which STK11 was restored into the wild type when both of the cell lines are treated with the cardiac glycosides for a long time.

[0109] As shown in FIG. 6, it was revealed that a growth inhibitory effect on the mutant-type cell line tended to increase, compared to the cell line in which STK11 was restored into the wild type, when both of the cell lines were treated with the cardiac glycosides for a long time (3 days, 7 days, and 14 days). Therefore, ATP1A1 inhibition using effective drugs may provide an effective treatment of the patient's tumor containing STK11 mutations.

[0110] These results showed that digoxin, digitoxin, or ouabain specifically inhibited the cell growth in the STK11 mutation cancer.

EXAMPLE 4: ANALYSIS OF INHIBITORY EFFECT SPECIFIC TO STK11-MUTANT LUNG CANCER ON CELL GROWTH BY ATP1A1 KNOCKDOWN

[0111] (1) SiRNA Transfection

[0112] For siRNA transfection, the cells were plated on a 96-well plate at a density of 3,000 cells/well. After the cells were attached for 24 hours, target siRNAs (ATP1A1: 1009769 (Bioneer); STK11: L-005035-00; and Non-targeting: D-001810-10 (Dharmacon)) were added to a transfection medium (GIBCO) at 37 C. for 6 hours in a CO.sub.2 incubator. After the transfection, an RPMI medium including FBS was further added to the cells, and the cells were then collected and cultured at 37 C., with CO.sub.2 for 72 hours in an incubator.

[0113] (2) Analysis of Correlation Between STK11 Mutations and ATP1A1 Expression in Lung Cancer

[0114] FIG. 7A shows TiterBlue results of evaluating cell viability obtained after four lung cancer cell lines are treated with ATP1A1 siRNA (for 72 hours).

[0115] From the results of FIG. 7A, it can be seen that the growth of the STK11-mutant lung cancer cell lines A549 and H460 were significantly inhibited, compared to the STK11-wild-type lung cancer cell lines H226 and H322, when the lung cancer cell lines were treated with the ATP1A1 siRNA. That is, when ATP1A1 was knocked down in a series of lung cancer cell lines, the cell growth was significantly reduced in the STK11-mutant cell lines rather than the STK11-wild-type cell lines. Also, FIG. 7B shows TiterBlue results of expressing wild-type STK11 in the STK11-mutant lung cancer cell lines A549 and H460. It can be seen that the cell growth was less reduced due to the ATP1A1 knockdown.

[0116] Therefore, ATP1A1 seems to play an important role in cancer survival or growth in the STK11-mutated lung cancer cell lines.

[0117] Next, FIG. 8 shows results of inhibiting the cell growth obtained by knocking down both ATP1A1 and STK11 (72 hours) in two lung cancer cell lines having wild-type STK11. It can be seen that the cell growth was synergistically inhibited in the STK11-wild-type lung cancer cell lines when both of ATP1A1 and STK11 were knocked down, compared to when either ATP1A1 or STK11 was knocked down.

EXAMPLE 5: INHIBITORY EFFECT OF CARDIAC GLYCOSIDES ON CELL MIGRATION AND DIVISION SPECIFIC TO STK11 MUTATIONS

[0118] The STK11-mutant lung cancer cell lines A549 and H460 (STK11 mutants) and the cell lines A549-STK11 and H460-STK11 in which STK11 was restored into the wild type (STK11 restored) were treated with the cardiac glycoside (digoxin, digitoxin, or ouabain) to evaluate an effect on cell migration and cell division.

[0119] For a cell migration assay, a Transwell cell culture chamber (Costar 3422, Cambridge, Mass.) equipped with a filter having a pore size of 12 m was used. More specifically, a cell suspension (510.sup.4 cells/500 l of a culture medium) was added to the top of the filter, and treated with each of the cardiac glycosides. After 24 hours, the cells migrating to the bottom of the filter were counted in 10 random fields using a phase-contrast microscope with 100 magnification. Also, a BrdU assay was used as the cell division assay. More specifically, the cells were inoculated in a 96-well plate at a density of 2,500 cells/well, treated with the cardiac glycoside (100 nM digoxin, 50 nM digitoxin, or 50 nM ouabain) after 24 hours, and then cultured again for 24 hours. Thereafter, the cells were labeled with bromodeoxyuridine (BrdU) for 2 hours. Then, the assay was performed by detecting the labeled cells using an ELISA reader (Cell Proliferation ELISA, BrdU (colorimetric), Roche).

[0120] As a result, as seen from the analysis results of the cell migration of FIG. 9A and the cell division of FIG. 9B, it can be seen that the cell migration and division were significantly decreasedwhen the STK11-mutant lung cancer cell lines were treated with the cardiac glycosides. The results indicate that the cardiac glycosides inhibited the migration and division of the STK11-mutant lung cancer cells.

EXAMPLE 6: STK11-MUTATION-SPECIFIC ANTICANCER EFFECTS OF CARDIAC GLYCOSIDES IN ANIMAL MODEL

[0121] To examine whether an ATP1A1 inhibitor had a preclinical effect on STK11-mutant lung cancer, this experiment was performed using the animal model in which an A549 lung cancer cell line or a cell line (A549-LKB1wt) in which STK11 was restored into the wild type was transplanted into mice (a mouse tumor xenograft model). After athymic nude mice (Oriental Bio Inc) were purchased, the animal model was prepared according to the standard guidelines provided by the Catholic University of Korea-Institutional Animal Care and Use Committee (CUK-IACUC). A549 or A549-LKB 1 wt were subcutaneously injected (310.sup.6 cells/ml) into the above animal model, and divided into three groups: (1) an untreated control group (n=10); (2) a group in which the mice were treated with digoxin at 60 ng/kg/body weight (n=10); (3) a group in which the mice were treated with digoxin at 180 ng/kg/body weight (n=10). Digoxin or a vehicle (1.9% DMSO/10% polyethylene glycol 400/lPBS: a total volume of 200 l) was orally administered three times a week for 5 weeks. Then, the diameter of each tumor base was measured, and the size of a tumor was then calculated according to the following equation: Tumor size (mm.sup.3)=(lengthwidthheight0.52). Also, the mice were monitored until the tumor size reached 1 cm.sup.3, and then the mice were sacrificed, and tumors were extracted from the mice.

[0122] FIG. 10A shows that the growth of a tumor in the animal model in which the A549 cell line was injected into the mice was reduced in a time-dependent manner when the cardiac glycoside (i.e., digoxin) was orally administered to the mice, and FIG. 10B shows results of determining that the cardiac glycoside did not have the same effect as described above in the animal model in which the cell line in which STK11 was restored into the wild type was injected into the mice.

[0123] Therefore, changes in the size of a tumor in the STK11 mutant types and the cell line in which STK11 was restored (wild-type STK11) were compared and analyzed. As shown in FIGS. 10C, 10D, and 10E, it can be seen that the tumor growth was selectively reduced by treatment with digoxin in the animal model in which the STK11-mutant cells were injected into the mice, compared to the animal model in which the wild-type STK11-expressed cells were injected into the mice. Interestingly, it was revealed that the selective sensitivities to the cardiac glycosides were significant when the cardiac glycosides was administered at a low drug dose [60 ng/ind. (3 g/kg)], compared to when the cardiac glycosides was administered at a high drug dose [180 ng/ind. (9 g/kg)]. While the concentration of the prescribed digoxin used in the conventional clinical trials was 250 mcg/day on average in the case of adults, it can be seen that an expected concentration of the cardiac glycoside to be prescribed for STK11-mutant-type lung cancer would be very low at 180 mcg/day or less on average in the case of adults.

[0124] The results indicate that the cardiac glycosides had a preclinical anti-cancer effect specific to the STK11-mutant lung cancer.

[0125] The present invention has been described in detail. However, it should be understood that the detailed description and specific examples, while indicating preferred embodiments of the invention, are given by way of illustration only, since various changes and modifications within the spirit and scope of the invention will become apparent to those skilled in the art from this detailed description.

INDUSTRIAL APPLICABILITY

[0126] The present invention can be applied to diagnosis or treatment of STK11-mutant lung cancer, and can be useful in developing therapeutic agents for treating STK11-mutant lung cancer.