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Editorial

Update on the role and therapeutic potential of polycomb repressive complexes in (biliary tract) cancer

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Pages 1-3 | Received 13 Sep 2017, Accepted 15 Nov 2017, Published online: 20 Nov 2017

References

  • Mayr C, Neureiter D, Wagner A, et al. The role of polycomb repressive complexes in biliary tract cancer. Expert Opin Ther Targets. 2015;19:363–375.
  • Sauvageau M, Sauvageau G. Polycomb group proteins: multi-faceted regulators of somatic stem cells and cancer. Cell Stem Cell. 2010;7:299–313.
  • Razumilava N, Gores GJ. Cholangiocarcinoma. Lancet. 2014;383:2168–2179.
  • Valle JW, Furuse J, Jitlal M, et al. Cisplatin and gemcitabine for advanced biliary tract cancer: a meta-analysis of two randomised trials. Ann Oncol. 2014;25:391–398.
  • Kreso A, Van Galen P, Pedley NM, et al. Self-renewal as a therapeutic target in human colorectal cancer. Nat Med. 2014;20:29–36.
  • Ma MZ, Chu BF, Zhang Y, et al. Long non-coding RNA CCAT1 promotes gallbladder cancer development via negative modulation of miRNA-218-5p. Cell Death Dis. 2015;6:e1583.
  • Mayr C, Wagner A, Loeffelberger M, et al. The BMI1 inhibitor PTC-209 is a potential compound to halt cellular growth in biliary tract cancer cells. Oncotarget. 2016;7:745–758.
  • Zhang P, Guo Z, Wu Y, et al. Histone deacetylase inhibitors inhibit the proliferation of gallbladder carcinoma cells by suppressing AKT/mTOR signaling. PLoS One. 2015;10:e0136193.
  • Srinivasan M, Bharali DJ, Sudha T, et al. Downregulation of Bmi1 in breast cancer stem cells suppresses tumor growth and proliferation. Oncotarget. 2017;8:38731–38742.
  • Bolomsky A, Schlangen K, Schreiner W, et al. Targeting of BMI-1 with PTC-209 shows potent anti-myeloma activity and impairs the tumour microenvironment. J Hematol Oncol. 2016;9:17.
  • Dimri M, Kang M, Dimri GP. A miR-200c/141-BMI1 autoregulatory loop regulates oncogenic activity of BMI1 in cancer cells. Oncotarget. 2016;7:36220–36234.
  • Kreso A, Dick JE. Evolution of the cancer stem cell model. Cell Stem Cell. 2014;14:275–291.
  • Zhang Z, Wang Q, Bu X, et al. Overexpression of Bmi1 promotes epithelialmesenchymal transition in CD133+Hep G2 cells. Mol Med Rep. 2017;16:6156–6161.
  • Jin X, Kim LJY, Wu Q, et al. Targeting glioma stem cells through combined BMI1 and EZH2 inhibition. Nat Med. 2017.
  • Mayr C, Ocker M, Ritter M, et al. Biliary tract cancer stem cells - translational options and challenges. World J Gastroenterol. 2017;23:2470–2482.
  • Sasaki M, Yamaguchi J, Ikeda H, et al. Polycomb group protein Bmi1 is overexpressed and essential in anchorage-independent colony formation, cell proliferation and repression of cellular senescence in cholangiocarcinoma: tissue and culture studies. Hum Pathol. 2009;40:1723–1730.
  • Mayr C, Beyreis M, Wagner A, et al. Deregulated MicroRNAs in biliary tract cancer: functional targets and potential biomarkers. Biomed Res Int. 2016;2016:4805270.
  • Urbas R, Mayr C, Klieser E, et al. Relevance of MicroRNA200 Family and MicroRNA205 for epithelial to mesenchymal transition and clinical outcome in biliary tract cancer patients. Int J Mol Sci. 2016;17(12).
  • Ma MZ, Li CX, Zhang Y, et al. Long non-coding RNA HOTAIR, a c-MYC activated driver of malignancy, negatively regulates miRNA-130a in gallbladder cancer. Mol Cancer. 2014;13:156.
  • Mayr C, Wagner A, Stoecklinger A, et al. 3-Deazaneplanocin A may directly target putative cancer stem cells in biliary tract cancer. Anticancer Res. 2015;35:4697–4705.
  • Gutschner T, Diederichs S. The hallmarks of cancer: a long non-coding RNA point of view. RNA Biol. 2012;9:703–719.

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