目的 總結(jié)雷帕霉素靶蛋白(mTOR)及其信號(hào)通路在胃癌化療耐藥中的研究現(xiàn)狀。
方法 查閱國(guó)內(nèi)外近年來(lái)有關(guān)mTOR信號(hào)通路在胃癌化療耐藥中作用機(jī)理的文獻(xiàn)并做綜述。
結(jié)果 mTOR作為mTOR信號(hào)轉(zhuǎn)導(dǎo)通路中一個(gè)重要的信號(hào)分子,參與了細(xì)胞的生長(zhǎng)、增殖以及代謝,血管新生等重要過(guò)程。mTOR信號(hào)通路相關(guān)分子在胃癌中過(guò)表達(dá),在胃癌的化療耐藥中起重要作用。此外,腫瘤干細(xì)胞也參與了胃癌的化療耐藥。
結(jié)論 mTOR及其信號(hào)通路在胃癌的化療耐藥中起重要作用。以mTOR為靶點(diǎn),聯(lián)合應(yīng)用mTOR抑制劑和化療藥物治療胃癌,對(duì)克服胃癌化療耐藥已初見(jiàn)成效,具有廣闊的臨床應(yīng)用前景。
引用本文: 朱優(yōu)龍,姜波健,俞繼衛(wèi). mTOR及其信號(hào)通路在胃癌化療耐藥中的研究進(jìn)展△. 中國(guó)普外基礎(chǔ)與臨床雜志, 2012, 19(12): 1352-1356. doi: 復(fù)制
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2. | Menges M, Hoehler T. Current strategies in systemic treatment of gastric cancer and cancer of the gastroesophageal junction[J].J Cancer Res Clin Oncol, 2009, 135(1):29-38. |
3. | Al-Batran SE, Ducreux M, Ohtsu A. mTOR as a therapeutic target in patients with gastric cancer[J]. Int J Cancer, 2012, 130(3):491-496. |
4. | Wander SA, Hennessy BT, Slingerland JM. Next-generation mTOR inhibitors in clinical oncology:how pathway complexity informs therapeutic strategy[J]. J Clin Invest, 2011, 121(4):1231-1241. |
5. | Sarbassov DD, Ali SM, Sabatini DM. Growing roles for the mTOR pathway[J]. Curr Opin Cell Biol, 2005, 17(6):596-603. |
6. | Yu G, Wang J, Chen Y, et al. Overexpression of phosphorylated mammalian target of rapamycin predicts lymph node metastasis and prognosis of Chinese patients with gastric cancer[J]. Clin Cancer Res, 2009, 15(5):1821-1829. |
7. | Kamata S, Kishimoto T, Kobayashi S, et al. Possible involvement of persistent activity of the mammalian target of rapamycin pathway in the cisplatin resistance of AFP-producing gastric cancercells[J]. Cancer Biol Ther, 2007, 6(7):1036-1043. |
8. | Lee KH, Hur HS, Im SA, et al. RAD001 shows activity against gastric cancer cells and overcomes 5-FU resistance by downregula-ting thymidylate synthase[J]. Cancer Lett, 2010, 299(1):22-28. |
9. | Semenza GL. HIF-1:upstream and downstream of cancer metab-olism[J]. Curr Opin Genet Dev, 2010, 20(1):51-56. |
10. | Nakamura J, Kitajima Y, Kai K, et al. Hypoxia-inducible factor-1alpha expression predicts the response to 5-fluorouracil-basedadjuvant chemotherapy in advanced gastric cancer[J]. Oncol Rep, 2009, 22(4):693-699. |
11. | Nakamura J, Kitajima Y, Kai K, et al. HIF-1alpha is an unfavor-able determinant of relapse in gastric cancer patients who underwent curative surgery followed by adjuvant 5-FU chemotherapy[J]. Int J Cancer, 2010, 127(5):1158-1171. |
12. | Rohwer N, Dame C, Haugstetter A, et al. Hypoxia-inducible factor 1α determines gastric cancer chemosensitivity via modulation of p53 and NF-κB[J]. PLoS One, 2010, 5(8):e12038. |
13. | Kim HK, Choi IJ, Kim CG, et al. A gene expression signature of acquired chemoresistance to cisplatin and fluorouracil combination chemotherapy in gastric cancer patients[J]. PLoS One, 2011, 6(2):e16694. |
14. | 姜海廣, 陸瑞祺, 吳巨鋼, 等. 基質(zhì)細(xì)胞源性因子-1α/CXC趨化因子受體-4軸經(jīng)PI3K/Akt通路對(duì)胃癌細(xì)胞CD133表達(dá)的調(diào)控作用[J]. 中華實(shí)驗(yàn)外科雜志, 2012, 29(3):378-380. |
15. | Anderson EC, Hessman C, Levin TG, et al. The role of colorectal cancer stem cells in metastatic disease and therapeutic response[J]. Cancer, 2011, 3(1):319-339. |
16. | Dirks P. Cancer stem cells:invitation to a second round[J].Nature, 2010, 466(7302):40-41. |
17. | Frank NY, Schatton T, Frank MH. The therapeutic promise of the cancer stem cell concept[J]. J Clin Invest, 2010, 120(1):41-50. |
18. | Shafee N, Smith CR, Wei Shuanzeng, et al. Cancer stem cells contribute to cisplatin resistance in Brca1/p53-mediated mouse mammary tumors[J]. Cancer Res, 2008, 68(9):3243-3250. |
19. | To K, Fotovati A, Reipas KM, et al. Y-box binding protein-1 induces the expression of CD44 and CD49f leading to enhanced self-renewal, mammosphere growth, and drug resistance[J]. Cancer Res, 2010, 70(7):2840-2851. |
20. | Cammareri P, Scopelliti A, Todaro M, et al. Aurora-a is essential for the tumorigenic capacity and chemoresistance of colorectal cancer stem cells[J]. Cancer Res, 2010, 70(11):4655-4665. |
21. | Zhang L, Jiao M, Li L, et al. Tumorspheres derived from prostate cancer cells possess chemoresistant and cancer stem cell properties[J]. J Cancer Res Clin Oncol, 2012, 138(4):675-686. |
22. | Jimeno A, Rudek MA, Kulesza P, et al. Pharmacodynamic-guided modified continuous reassessment method-based, dose-finding study of rapamycin in adult patients with solid tumors[J]. J Clin Oncol, 2008, 26(25):4172-4179. |
23. | Hashimoto I, Koizumi K, Tatematsu M, et al. Blocking on the CXCR4/mTOR signaling pathway induces the anti-metastatic properties and autophagic cell death in peritoneal disseminated gastric cancer cells[J]. Eur J Cancer, 2008, 44(7):1022-1029. |
24. | Cejka D, Preusser M, Fuereder T, et al. mTOR inhibition sensitizes gastric cancer to alkylating chemotherapy in vivo[J]. Anticancer Res, 2008, 28(6A):3801-3808. |
25. | Cejka D, Preusser M, Woehrer A, et al. Everolimus (RAD001) and anti-angiogenic cyclophosphamide show long-term control of gastric cancer growth in vivo[J]. Cancer Biol Ther, 2008, 7(9):1377-1385. |
26. | Feldman ME, Apsel B, Uotila A, et al. Active-site inhibitors of mTOR target rapamycin-resistant outputs of mTORC1 and mTORC2[J]. PLoS Biol, 2009, 7(2):e1000038. |
27. | Choo AY, Yoon SO, Kim SG, et al. Rapamycin differentially inhibits S6Ks and 4E-BP1 to mediate cell-type-specific repression of mRNA translation[J]. Proc Natl Acad Sci U S A, 2008, 105(45):17414-17419. |
28. | Thoreen CC, Kang SA, Chang JW, et al. An ATP-competitive mammalian target of rapamycin inhibitor reveals rapamycin-resistant functions of mTORC1[J]. J Biol Chem, 2009, 284(12):8023-8032. |
29. | O’reilly KE, Rojo F, She QB, et al. mTOR inhibition induces upstream receptor tyrosine kinase signaling and activates Akt[J]. Cancer Res, 2006, 66(3):1500-1508. |
30. | Breuleux M, Klopfenstein M, Stephan C, et al. Increased Akt S473 phosphorylation after mTORC1 inhibition is rictor dependent and does not predict tumor cell response to PI3K/mTOR inhibition[J]. Mol Cancer Ther, 2009, 8(4):742-753. |
31. | García-Martínez JM, Moran J, Clarke RG, et al. Ku-0063794 is a specific inhibitor of the mammalian target of rapamycin (mTOR)[J]. Biochem J, 2009, 421(1):29-42. |
32. | Chresta CM, Davies BR, Hickson I, et al. AZD8055 is a potent, selective, and orally bioavailable ATP-competitive mammalian target of rapamycin kinase inhibitor with in vitro and in vivo antitumor activity[J]. Cancer Res, 2010, 70(1):288-298. |
33. | Yu K, Shi C, Toral-Barza L, et al. Beyond rapalog therapy:preclinical pharmacology and antitumor activity of WYE-125132, an ATP-competitive and specific inhibitor of mTORC1 and mTORC2[J]. Cancer Res, 2010, 70(2):621-631. |
34. | Bhagwat SV, Gokhale PC, Crew AP, et al. Preclinical characterization of OSI-027, a potent and selective inhibitor of mTORC1 and mTORC2:distinct from rapamycin[J]. Mol Cancer Ther, 2011, 10(8):1394-1406. |
35. | Füreder T, Wanek T, Pflegerl P, et al. BEZ235 impairs gastriccancer growth by inhibition of PI3K/mTOR in vitro and in vivo[J]. BMC Pharmacol, 2010, 10(Suppl 1):A41. |
- 1. Lin Y, Ueda J, Kikuchi S, et al. Comparative epidemiology of gastric cancer between Japan and China[J]. World J Gastroenterol, 2011, 17(39):4421-4428.
- 2. Menges M, Hoehler T. Current strategies in systemic treatment of gastric cancer and cancer of the gastroesophageal junction[J].J Cancer Res Clin Oncol, 2009, 135(1):29-38.
- 3. Al-Batran SE, Ducreux M, Ohtsu A. mTOR as a therapeutic target in patients with gastric cancer[J]. Int J Cancer, 2012, 130(3):491-496.
- 4. Wander SA, Hennessy BT, Slingerland JM. Next-generation mTOR inhibitors in clinical oncology:how pathway complexity informs therapeutic strategy[J]. J Clin Invest, 2011, 121(4):1231-1241.
- 5. Sarbassov DD, Ali SM, Sabatini DM. Growing roles for the mTOR pathway[J]. Curr Opin Cell Biol, 2005, 17(6):596-603.
- 6. Yu G, Wang J, Chen Y, et al. Overexpression of phosphorylated mammalian target of rapamycin predicts lymph node metastasis and prognosis of Chinese patients with gastric cancer[J]. Clin Cancer Res, 2009, 15(5):1821-1829.
- 7. Kamata S, Kishimoto T, Kobayashi S, et al. Possible involvement of persistent activity of the mammalian target of rapamycin pathway in the cisplatin resistance of AFP-producing gastric cancercells[J]. Cancer Biol Ther, 2007, 6(7):1036-1043.
- 8. Lee KH, Hur HS, Im SA, et al. RAD001 shows activity against gastric cancer cells and overcomes 5-FU resistance by downregula-ting thymidylate synthase[J]. Cancer Lett, 2010, 299(1):22-28.
- 9. Semenza GL. HIF-1:upstream and downstream of cancer metab-olism[J]. Curr Opin Genet Dev, 2010, 20(1):51-56.
- 10. Nakamura J, Kitajima Y, Kai K, et al. Hypoxia-inducible factor-1alpha expression predicts the response to 5-fluorouracil-basedadjuvant chemotherapy in advanced gastric cancer[J]. Oncol Rep, 2009, 22(4):693-699.
- 11. Nakamura J, Kitajima Y, Kai K, et al. HIF-1alpha is an unfavor-able determinant of relapse in gastric cancer patients who underwent curative surgery followed by adjuvant 5-FU chemotherapy[J]. Int J Cancer, 2010, 127(5):1158-1171.
- 12. Rohwer N, Dame C, Haugstetter A, et al. Hypoxia-inducible factor 1α determines gastric cancer chemosensitivity via modulation of p53 and NF-κB[J]. PLoS One, 2010, 5(8):e12038.
- 13. Kim HK, Choi IJ, Kim CG, et al. A gene expression signature of acquired chemoresistance to cisplatin and fluorouracil combination chemotherapy in gastric cancer patients[J]. PLoS One, 2011, 6(2):e16694.
- 14. 姜海廣, 陸瑞祺, 吳巨鋼, 等. 基質(zhì)細(xì)胞源性因子-1α/CXC趨化因子受體-4軸經(jīng)PI3K/Akt通路對(duì)胃癌細(xì)胞CD133表達(dá)的調(diào)控作用[J]. 中華實(shí)驗(yàn)外科雜志, 2012, 29(3):378-380.
- 15. Anderson EC, Hessman C, Levin TG, et al. The role of colorectal cancer stem cells in metastatic disease and therapeutic response[J]. Cancer, 2011, 3(1):319-339.
- 16. Dirks P. Cancer stem cells:invitation to a second round[J].Nature, 2010, 466(7302):40-41.
- 17. Frank NY, Schatton T, Frank MH. The therapeutic promise of the cancer stem cell concept[J]. J Clin Invest, 2010, 120(1):41-50.
- 18. Shafee N, Smith CR, Wei Shuanzeng, et al. Cancer stem cells contribute to cisplatin resistance in Brca1/p53-mediated mouse mammary tumors[J]. Cancer Res, 2008, 68(9):3243-3250.
- 19. To K, Fotovati A, Reipas KM, et al. Y-box binding protein-1 induces the expression of CD44 and CD49f leading to enhanced self-renewal, mammosphere growth, and drug resistance[J]. Cancer Res, 2010, 70(7):2840-2851.
- 20. Cammareri P, Scopelliti A, Todaro M, et al. Aurora-a is essential for the tumorigenic capacity and chemoresistance of colorectal cancer stem cells[J]. Cancer Res, 2010, 70(11):4655-4665.
- 21. Zhang L, Jiao M, Li L, et al. Tumorspheres derived from prostate cancer cells possess chemoresistant and cancer stem cell properties[J]. J Cancer Res Clin Oncol, 2012, 138(4):675-686.
- 22. Jimeno A, Rudek MA, Kulesza P, et al. Pharmacodynamic-guided modified continuous reassessment method-based, dose-finding study of rapamycin in adult patients with solid tumors[J]. J Clin Oncol, 2008, 26(25):4172-4179.
- 23. Hashimoto I, Koizumi K, Tatematsu M, et al. Blocking on the CXCR4/mTOR signaling pathway induces the anti-metastatic properties and autophagic cell death in peritoneal disseminated gastric cancer cells[J]. Eur J Cancer, 2008, 44(7):1022-1029.
- 24. Cejka D, Preusser M, Fuereder T, et al. mTOR inhibition sensitizes gastric cancer to alkylating chemotherapy in vivo[J]. Anticancer Res, 2008, 28(6A):3801-3808.
- 25. Cejka D, Preusser M, Woehrer A, et al. Everolimus (RAD001) and anti-angiogenic cyclophosphamide show long-term control of gastric cancer growth in vivo[J]. Cancer Biol Ther, 2008, 7(9):1377-1385.
- 26. Feldman ME, Apsel B, Uotila A, et al. Active-site inhibitors of mTOR target rapamycin-resistant outputs of mTORC1 and mTORC2[J]. PLoS Biol, 2009, 7(2):e1000038.
- 27. Choo AY, Yoon SO, Kim SG, et al. Rapamycin differentially inhibits S6Ks and 4E-BP1 to mediate cell-type-specific repression of mRNA translation[J]. Proc Natl Acad Sci U S A, 2008, 105(45):17414-17419.
- 28. Thoreen CC, Kang SA, Chang JW, et al. An ATP-competitive mammalian target of rapamycin inhibitor reveals rapamycin-resistant functions of mTORC1[J]. J Biol Chem, 2009, 284(12):8023-8032.
- 29. O’reilly KE, Rojo F, She QB, et al. mTOR inhibition induces upstream receptor tyrosine kinase signaling and activates Akt[J]. Cancer Res, 2006, 66(3):1500-1508.
- 30. Breuleux M, Klopfenstein M, Stephan C, et al. Increased Akt S473 phosphorylation after mTORC1 inhibition is rictor dependent and does not predict tumor cell response to PI3K/mTOR inhibition[J]. Mol Cancer Ther, 2009, 8(4):742-753.
- 31. García-Martínez JM, Moran J, Clarke RG, et al. Ku-0063794 is a specific inhibitor of the mammalian target of rapamycin (mTOR)[J]. Biochem J, 2009, 421(1):29-42.
- 32. Chresta CM, Davies BR, Hickson I, et al. AZD8055 is a potent, selective, and orally bioavailable ATP-competitive mammalian target of rapamycin kinase inhibitor with in vitro and in vivo antitumor activity[J]. Cancer Res, 2010, 70(1):288-298.
- 33. Yu K, Shi C, Toral-Barza L, et al. Beyond rapalog therapy:preclinical pharmacology and antitumor activity of WYE-125132, an ATP-competitive and specific inhibitor of mTORC1 and mTORC2[J]. Cancer Res, 2010, 70(2):621-631.
- 34. Bhagwat SV, Gokhale PC, Crew AP, et al. Preclinical characterization of OSI-027, a potent and selective inhibitor of mTORC1 and mTORC2:distinct from rapamycin[J]. Mol Cancer Ther, 2011, 10(8):1394-1406.
- 35. Füreder T, Wanek T, Pflegerl P, et al. BEZ235 impairs gastriccancer growth by inhibition of PI3K/mTOR in vitro and in vivo[J]. BMC Pharmacol, 2010, 10(Suppl 1):A41.