Versatile inhibitory effects of the flavonoid-derived PI3K/Akt inhibitor, LY294002, on ATP-binding cassette transporters that characterize stem cells
© Imai et al.; licensee Springer. 2012
Received: 4 July 2012
Accepted: 9 October 2012
Published: 13 October 2012
Stem cells are undifferentiated cells capable of proliferation, self-renewal, and production of a large number of differentiated progeny. Stem cells exist even in malignancies. They are called cancer stem cells, which may represent the origin of these tumors and may be one of the reasons of chemoresistance. The phosphatidylinositol-3-kinase (PI3K)/Akt pathway is important for the maintenance of pluripotency in stem cells. Flow cytometry assay for identifying stem cells defines a side population of cells that displays low fluorescent dye and is highly enriched for stem cells. The dye efflux is attributed to expression of ATP-binding cassette transporters such as P-glycoprotein and breast cancer resistance protein (BCRP)/ABCG2, which also transport a variety of anticancer drugs. The PI3K/Akt pathway can modulate functions of ABC transporters through various mechanisms. Reportedly, inhibition of the PI3K/Akt pathway caused BCRP translocation in hematopoietic stem cells and glioma stem-like cells. On the other hand, a PI3K inhibitor, LY294002, reversed multidrug resistance in cancer cells that overexpress BCRP not by affecting BCRP translocation but putatively as a competitive inhibitor. Other PI3K inhibitors, wortmannin and PI-103, did not reverse BCRP-mediated drug resistance. Since LY294002 is a derivative of quercetin that is a naturally occurring flavonoid, its chemical structure is similar to those of a group of flavonoids but those of wortmannin and PI-103 are quite different. It is known that many flavonoids are inhibitors of BCRP and PI3K. LY294002 has also been reported to exert inhibitory effects on multidrug resistance-associated protein 1 (MRP1) function via dual mechanisms, competitive block of substrate transport and modulation of expression. Furthermore, LY294002 has been found to antagonize transport activity of P-glycoprotein without influencing its expression. Taken together, LY294002 can inhibit all BCRP, P-glycoprotein, and MRP1, which are three major ABC transporters that are highly expressed in stem cells and cause multidrug resistance. Due to its versatile effects, LY294002 could be a lead compound for developing more effective and tolerable reagents for cancer treatment.
KeywordsABC transporter BCRP P-glycoprotein MRP1 PI3K/Akt LY294002 Chemotherapy Stem cell
Stem cells are undifferentiated cells capable of proliferation, self-renewal, production of a large number of differentiated progeny, and regeneration of tissues . In addition to embryonic stem (ES) cells, stem cells also exist in various adult tissues such as skin, bone marrow, liver, striated muscle, and brain . After tissue damage, they not only replenish the tissue they originally resided but also may contribute to repair another tissue. Cells with stem-cell qualities have also been identified in malignancies of hematopoietic origin and in some solid tumors . The cells, called cancer stem cells or cancer stem-like cells, share many properties of normal stem cell, such as relative quiescence, resistance to drugs and toxins, an active DNA-repair capacity, and a resistance to apoptosis, thus providing for a long lifespan.
For decades, the unregulated growth of cancers was attributed to the serial acquisition of genetic events that resulted in the activation of oncogenes and silencing of tumor suppressor genes involved in apoptosis. Now, it is recognized that another key event in tumor progression is the alterations of genes involved in regulation of stem cell renewal. When cancer cells of different origins were analyzed for their proliferative potential in various assays, only a small minority of cells were able to proliferate extensively. Those cells, i.e., cancer stem cells, are derived either from transformed normal stem cells or more differentiated progenitor cells that have acquired the ability of self-renewal as a result of oncogenic mutation . Thus, cancer stem cells may represent the origin of cancer and furthermore would play a pivotal role in maintaining cancer cell population. In this point of view, characterization of cancer stem cells would be significant and important for clinical cancer treatment.
Stem cells can be purified based on the efflux of fluorescent dyes such as rhodamine 123 (rho123) and Hoechst 33342 (Hoechst). A widely used flow cytometry assay for identifying stem cells defines a side population (SP) of cells displaying low Hoechst fluorescence and comprising about 0.05% of total cells . This SP population is highly enriched for lineage-specific stem cells. The dye efflux component of the SP phenotype has been assumed to express ATP-binding cassette (ABC) transporters such as P-glycoprotein (P-gp), encoded by the multidrug resistance 1 (MDR1) gene, and breast cancer resistance protein (BCRP)/ABCG2. BCRP expels Hoechst but not rho123, while P-gp expels both Hoechst and rho123. Accordingly, normal and cancer stem cells express high levels of P-gp and BCRP. These two ABC transporters and multidrug resistance-associated protein 1 (MRP1)/ABCC1 constitute the three principle ABC transporters implicated in multidrug resistance. MRP1 has also been found to be expressed in SP cells .
Chemoresistance and cancer stem cells
Cancer cells can acquire resistance to chemotherapy by various mechanisms. Since most cancer cells are genetically unstable at either chromosomal or nucleotide level, cancer cells that recur after initial chemotherapy usually acquire drug resistance by accumulating genetic changes which lead to a selective advantage that allows them to survive the chemotherapy and reconstitute the population of tumor cells. Some of these genetic changes observed in cancer cells grown in tissue culture are a loss of cell surface receptor or transporter for a drug, specific metabolism of a drug, or alteration by mutation of the specific target of a drug. In such cases, resistance to only a small number of related drugs is observed. In addition, cancer cells often express mechanisms that confer simultaneous resistance to many structurally and functionally unrelated drugs. This phenomenon, called multidrug resistance, can result from limitation of cellular drug accumulation by limiting uptake, enhancing efflux or affecting membrane lipids such as ceramid . Blocking apoptosis, activation of detoxifying drugs, repair of DNA damage, and alteration in the cell cycle and checkpoints also render cancer cells resistant to the cytotoxic drugs . Alternatively, cancer stem cells are intrinsically resistant to chemotherapy through their quiescence, their capacity for DNA repair, and expression of ABC transporters such as BCRP, P-gp, and MRP1. Cancer stem cells survive chemotherapy and support regrowth of the tumor. Those ABC transporters transport both hydrophobic and hydrophilic compounds, and play important roles in normal physiology in the transport of drugs . Therefore, modifying functions of the ABC transporters would be one of the attractive strategies for overcoming multidrug resistance of cancer stem cells.
The PI3K/Akt pathway in cancer stem cells
Large scale transcriptional profiling analysis revealed that many of the transcripts enriched in human ES cells fell within three major signaling categories belonging to the Ras/MAPK/ERK pathway, the phosphatidylinositol-3-kinase (PI3K)/Akt pathway, and NFκB signaling pathways . Among these, the PI3K/Akt pathway had been shown to be important for the maintenance of pluripotency in mouse ES cells [8, 9]. LY294002, which is a specific PI3K inhibitor, was shown to cause prominent cell differentiation in human ES cells . PI3K enzymes are normally regulated by growth factors and serve to phosphorylate phospholipids at the plasma membrane. Activated PI3K phosphorylates phosphatidylinositol 4,5-bisphosphate (PIP2) and generates phosphatidylinositol 3,4,5-triphosphate (PIP3) which acts as a second messenger. Akt interacts with PIP3 and subsequently translocates to the plasma membrane. Akt plays a critical role in controlling the balance between survival and apoptosis. Recent studies indicate that numerous components of the PI3K/Akt pathway are targeted by amplification, mutation and translocation more frequently than any other pathway in cancer patients, with resultant activation of the pathway . In addition, it has been suggested that activation of the PI3K/Akt pathway is required for the maintenance and viability of cancer stem cells in breast cancer, prostate cancer, and brain tumor [11–13]. Inhibition of AKT activity in cancer stem cells also resulted in sensitization of cells to therapy and increased survival of mice bearing human glioma xenografts in vivo [11–14]. Hence, the PI3K/Akt pathway can be an attractive target for cancer therapy. Inhibiting the pathway might also result in differentiation of cancer stem cells .
Inhibitor of PI3K internalizes BCRP in stem cells
The PI3K/Akt pathway can modulate functions of ABC transporters through various mechanisms. According to the previous studies, inhibition of the PI3K/Akt pathway caused BCRP internalization in cells. Mogi, et al. reported a reduced SP fraction in the bone marrow of Akt1-null mice . Enforced expression of Akt increased the SP fraction in the wild-type mouse bone marrow but not in the Bcrp−/− bone marrow. They also showed that treatment of SP cells with 10 μM of LY294002 for 90 min promoted Bcrp translocation from the plasma membrane to the intracellular compartment. Similar results have been reported concerning glioma tumor stem-like cells . However, the more detailed molecular mechanism of vesicular BCRP trafficking regulated by the PI3K/Akt pathway mostly remains to be elucidated. Alteration of subcellular BCRP localization was also observed in porcine non-SP cells, LLC-PK1 . Treatment with 20 μM of LY294002 for 90 min caused BCRP internalization from the cell surface. Transfection of the dominant-negative Akt plasmid resulted in internalization of a part of BCRP in LLC-PK1 cells. Therefore, it was hypothesized that cellular distribution of BCRP might be regulated by the PI3K/Akt signaling pathway in non-stem cells as well as stem cells.
LY294002 inhibits BCRP without affecting its translocation
For the past decade, PI3K/Akt inhibitors have been known to cause more favorable outcomes when co-administered with usual anticancer drugs. Deregulation of drug transporters is one of the postulated mechanisms. It had been reported that inhibition of the PI3K/Akt pathway modulated BCRP-mediated drug transport via BCRP translocation in SP cells in the bone marrow and glioma stem-like cells. It was also reported that inhibition of the PI3K/Akt pathway resulted in BCRP translocation in renal polarized cells [16–18]. However, effects of the PI3K/Akt inhibitors on BCRP function were found to be considerably different in BCRP-transfected MCF-7 cells. LY294002 did not affect cellular BCRP distribution in the cancer cell line but exerted inhibitory effects on BCRP-mediated topotecan efflux. Thus, LY294002 demonstrated BCRP-inhibitory effects different from those observed in the previous studies. Then, two possible explanations were postulated to explain the results. The first one was the difference of cell characters between stem cells and non-stem cells. Regulation of subcellular BCRP distribution by the PI3K/Akt pathway might be specific to a subset of cells such as stem/stem-like cells. It is known that the PI3K/Akt signaling pathway is activated and plays a role in the maintenance of pluripotency and viability of stem cells . BCRP is expressed on the cell surface of pluripotent stem cells but becomes downregulated with cell maturation. On the other hand, the PI3K/Akt signals have been reported to regulate activity and trafficking of some transporters and/or receptors, such as transferrin receptor, low-density lipoprotein receptor, the amino-acid transporter 4F2, integrin, and Glut1 through regulating endocytosis and recycling [20, 21]. Therefore, the PI3K/Akt signaling pathway might be involved in mechanisms of BCRP trafficking to the cell surface and maintenance of the pluripotency of stem cells. Another explanation was that some of the BCRP protein might be internalized, but expression levels of overexpessed BCRP in cancer cells are too high to discern internalized BCRP and most of BCRP would be left uninternalized. But, it was supposed that this hypothesis could not successfully explain the data that LY294002 clearly and remarkably sensitized MCF-7/BCRP cells to BCRP-substrate drugs. Accordingly, interaction of LY294002 with the drug binding sites of BCRP was thought to explain the reversal effects. Since BCRP overexpression did not result in acquisition of comparable degrees of LY294002 resistance with those of anticancer drugs (Figure 1C), LY294002 would not be a transport substrate of BCRP but it would competitively interact with the drug binding site.
Inhibitory effects of LY294002 on MRP1 and P-gp
LY294002 has been reported to competitively inhibit MRP1-mediated doxorubicin transport . Besides, MRP1 expression has been found to be regulated by the PI3K/Akt pathway. Treatment of myelogenous leukemia cells with wortmannin resulted in lower levels of phosphorylated Akt, downregulated MRP1 expression, and decreased rho123 extrusion in dye efflux assay . In another report, modulation of PI3K activity with the use of constitutively active and dominant-negative inhibitors was found to affect the ability of prostate cancer cells to respond to chemotoxic treatments . MRP1 expression was upregulated as a consequence of PI3K activation in prostate cancer cells. Thus, LY294002 can also exert inhibitory effects on MRP1 function via dual mechanisms, i.e., competitive block of substrate transport and modulation of expression.
LY294002 has also been observed to antagonize transport activity of P-gp without influencing its expression and antagonize P-gp-mediated multidrug resistance . Authors of this report discussed that suppression of the apoptotic pathway and regulation mechanism of the transport activity controlled by the PI3K/Akt kinase pathway might be additive to P-gp-mediated drug resistance. However, effects of other inhibitors of the pathway were not tested in the report, and we suspect that inhibition of P-gp-mediated drug transport by LY294002 might have been irrelevant to inhibition of the PI3K/Akt pathway. Taken together, LY294002 can inhibit all P-gp, MRP1 and BCRP.
Flavonoid as seeds of cancer chemotherapeutic drugs
- ES cells:
Embryonic stem cells
Multidrug resistance 1
Breast cancer resistance protein
Multidrug resistance-associated protein 1
We greatly appreciate Ms. Yoshimori M and staffs of Joint Research Center, Dokkyo Medical University Koshigaya Hospital for their technical assistance.
- Blau HM, Brazelton TR, Weimann JM: The evolving concept of a stem cell: entity or function? Cell 2001, 105: 829–841. 10.1016/S0092-8674(01)00409-3View ArticlePubMed
- Dean M, Fojo T, Bates S: Tumour stem cells and drug resistance. Nat Rev Cancer 2005, 5: 275–284. 10.1038/nrc1590View ArticlePubMed
- Bjerkvig R, Tysnes BB, Aboody KS, Najbauer J, Terzis AJ: Opinion: the origin of the cancer stem cell: current controversies and new insights. Nat Rev Cancer 2005, 5: 899–904. 10.1038/nrc1740View ArticlePubMed
- Zhou S, Schuetz JD, Bunting KD, Colapietro AM, Sampath J, Morris JJ, Lagutina I, Grosveld GC, Osawa M, Nakauchi H, Sorrentino BP: The ABC transporter Bcrp1/ABCG2 is expressed in a wide variety of stem cells and is a molecular determinant of the side-population phenotype. Nat Med 2001, 7: 1028–1034. 10.1038/nm0901-1028View ArticlePubMed
- Liu YY, Han TY, Giuliano AE, Cabot MC: Ceramide glycosylation potentiates cellular multidrug resistance. FASEB J 2001, 15: 719–730. 10.1096/fj.00-0223comView ArticlePubMed
- Gottesman MM: Mechanisms of cancer drug resistance. Annu Rev Med 2002, 53: 615–627. 10.1146/annurev.med.53.082901.103929View ArticlePubMed
- Armstrong L, Hughes O, Yung S, Hyslop L, Stewart R, Wappler I, Peters H, Walter T, Stojkovic P, Evans J, Stojkovic M, Lako M: The role of PI3K/AKT, MAPK/ERK and NFkappabeta signalling in the maintenance of human embryonic stem cell pluripotency and viability highlighted by transcriptional profiling and functional analysis. Hum Mol Genet 2006, 15: 1894–1913. 10.1093/hmg/ddl112View ArticlePubMed
- Takahashi K, Murakami M, Yamanaka S: Role of the phosphoinositide 3-kinase pathway in mouse embryonic stem (ES) cells. Biochem Soc Trans 2005, 33: 1522–1525. 10.1042/BST20051522View ArticlePubMed
- Paling NR, Wheadon H, Bone HK, Welham MJ: Regulation of embryonic stem cell self-renewal by phosphoinositide 3-kinase-dependent signaling. J Biol Chem 2004, 279: 48063–48070. 10.1074/jbc.M406467200View ArticlePubMed
- Hennessy BT, Smith DL, Ram PT, Lu Y, Mills GB: Exploiting the PI3K/AKT pathway for cancer drug discovery. Nat Rev Drug Discov 2005, 4: 988–1004. 10.1038/nrd1902View ArticlePubMed
- Zhou J, Wulfkuhle J, Zhang H, Gu P, Yang Y, Deng J, Margolick JB, Liotta LA, Petricoin E 3rd, Zhang Y: Activation of the PTEN/mTOR/STAT3 pathway in breast cancer stem-like cells is required for viability and maintenance. Proc Natl Acad Sci USA 2007, 104: 16158–16163. 10.1073/pnas.0702596104PubMed CentralView ArticlePubMed
- Hambardzumyan D, Becher OJ, Rosenblum MK, Pandolfi PP, Manova-Todorova K, Holland EC: PI3K pathway regulates survival of cancer stem cells residing in the perivascular niche following radiation in medulloblastoma in vivo. Genes Dev 2008, 22: 436–448. 10.1101/gad.1627008PubMed CentralView ArticlePubMed
- Dubrovska A, Kim S, Salamone RJ, Walker JR, Maira SM, García-Echeverría C, Schultz PG, Reddy VA: The role of PTEN/Akt/PI3K signaling in the maintenance and viability of prostate cancer stem-like cell populations. Proc Natl Acad Sci USA 2009, 106: 268–273. 10.1073/pnas.0810956106PubMed CentralView ArticlePubMed
- Eyler CE, Foo WC, LaFiura KM, McLendon RE, Hjelmeland AB, Rich JN: Brain cancer stem cells display preferential sensitivity to Akt inhibition. Stem Cells 2008, 26: 3027–3036. 10.1634/stemcells.2007-1073PubMed CentralView ArticlePubMed
- Massard C, Deutsch E, Soria JC: Tumour stem cell-targeted treatment: elimination or differentiation. Ann Oncol 2006, 17: 1620–1624. 10.1093/annonc/mdl074View ArticlePubMed
- Mogi M, Yang J, Lambert JF, Colvin GA, Shiojima I, Skurk C, Summer R, Fine A, Quesenberry PJ, Walsh K: Akt signaling regulates side population cell phenotype via Bcrp translocation. J Biol Chem 2003, 278: 39068–39075. 10.1074/jbc.M306362200View ArticlePubMed
- Bleau AM, Hambardzumyan D, Ozawa T, Fomchenko EI, Huse JT, Brennan CW, Holland EC: PTEN/PI3K/Akt pathway regulates the side population phenotype and ABCG2 activity in glioma tumor stem-like cell. Cell Stem Cell 2009, 4: 226–235. 10.1016/j.stem.2009.01.007PubMed CentralView ArticlePubMed
- Takada T, Suzuki H, Gotoh Y, Sugiyama Y: Regulation of the cell surface expression of human BCRP/ABCG2 by the phosphorylation state of Akt in polarized cells. Drug Meta Dispos 2005, 33: 905–909. 10.1124/dmd.104.003228View Article
- Imai Y, Yoshimori M, Fukuda K, Yamagishi H, Ueda Y: The PI3K/Akt inhibitor LY294002 reverses BCRP-mediated drug resistance without affecting BCRP translocation. Oncol Rep 2012, 27: 1703–1709.PubMed
- Wieman HL, Wofford JA, Rathmell JC: Cytokine stimulation promotes glucose uptake via phosphatidylinositol-3 kinase/Akt regulation of Glut1 activity and trafficking. Mol Biol Cell 2007, 18: 1437–1446. 10.1091/mbc.E06-07-0593PubMed CentralView ArticlePubMed
- Edinger AL, Thompson CB: Akt maintains cell size and survival by increasing mTOR-dependent nutrient uptake. Mol Biol Cell 2002, 13: 2276–2288. 10.1091/mbc.01-12-0584PubMed CentralView ArticlePubMed
- Abdul-Ghani R, Serra V, Györffy B, Jürchott K, Solf A, Schäfer R: The PI3K inhibitor LY294002 blocks drug export from resistant colon carcinoma cells overexpressing MRP1. Oncogene 2006, 25: 1743–1752. 10.1038/sj.onc.1209201View ArticlePubMed
- Tazzari PL, Cappellini A, Ricci F, Evangelisti C, Papa V, Grafone T, Martinelli G, Conte R, Cocco L, McCubrey JA, Martelli AM: Multidrug resistance-associated protein 1 expression is under the control of the phosphoinositide 3 kinase/Akt signal transduction network in human acute myelogenous leukemia blasts. Leukemia 2007, 21: 427–438. 10.1038/sj.leu.2404523View ArticlePubMed
- Lee JT Jr, Steelman LS, McCubrey JA: Phosphatidylinositol 3'-kinase activation leads to multidrug resistance protein-1 expression and subsequent chemoresistance in advanced prostate cancer cells. Cancer Res 2004, 64: 8397–8404. 10.1158/0008-5472.CAN-04-1612View ArticlePubMed
- Barancík M, Bohácová V, Sedlák J, Sulová Z, Breier A: LY294,002, a specific inhibitor of PI3K/Akt kinase pathway, antagonizes P-glycoprotein-mediated multidrug resistance. Eur J Pharm Sci 2006, 29: 426–434. 10.1016/j.ejps.2006.08.006View ArticlePubMed
- Imai Y, Tsukahara S, Asada S, Sugimoto Y: Phytoestrogens/flavonoids reverse breast cancer resistance protein /ABCG2 - mediated multidrug resistance. Cancer Res 2004, 64: 4346–4352. 10.1158/0008-5472.CAN-04-0078View ArticlePubMed
- Srivastava AK: Inhibition of phosphorylase kinase, and tyrosine protein kinase activities by quercetin. Biochem Biophys Res Commun 1985, 131: 1–5. 10.1016/0006-291X(85)91761-9View ArticlePubMed
- Agullo G, Gamet-Payrastre L, Manenti S, Viala C, Rémésy C, Chap H, Payrastre B: Relationship between flavonoid structure and inhibition of phosphatidylinositol 3-kinase: a comparison with tyrosine kinase and protein kinase C inhibition. Biochem Pharmacol 1997, 53: 1649–1657. 10.1016/S0006-2952(97)82453-7View ArticlePubMed
- Kong D, Zhang Y, Yamori T, Duan H, Jin M: Inhibitory activity of flavonoids against class I phosphatidylinositol 3-kinase isoforms. Molecules 2011, 16: 5159–5167. 10.3390/molecules16065159View ArticlePubMed
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.