Literature DB >> 21542457

Antitumor effect of suberoylanilide hydroxamic acid and topotecan in renal cancer cells.

Akinori Sato1, Takako Asano, Akio Horiguchi, Keiichi Ito, Makoto Sumitomo, Tomohiko Asano.   

Abstract

The treatment modality for advanced renal cancer is limited. The development of novel systemic therapies has long been waited for. Suberoylanilide hydroxamic acid (SAHA) is one of the most potent histone deacetylase (HDAC) inhibitors, which are promising novel anticancer agents. SAHA has already been tested in phase II clinical trials; however, its effectiveness has been found to be limited. Recently, the combination of SAHA and topoisomerase I inhibitor, topotecan, was shown to be effective, but this treatment strategy has not been tested in renal cancer cells. In the present study, we found that the combination of SAHA and topotecan effectively inhibited the growth of renal cancer cells by suppressing the expression of cyclin-dependent kinase (CDK) 4 and cyclin D1, and promoting retinoblastoma protein (Rb) dephosphorylation. Furthermore, the combination therapy was found to inhibit both the function and expression of HDACs, which may be one of the main mechanisms of the combination therapy. To the best of our knowledge, this is the first report that has revealed the combined beneficial effect of SAHA and topotecan on renal cancer cells. Combining SAHA and topotecan is thus a promising approach to the treatment of renal cancer.

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Year:  2011        PMID: 21542457     DOI: 10.3727/096504011x12970940207841

Source DB:  PubMed          Journal:  Oncol Res        ISSN: 0965-0407            Impact factor:   5.574


  5 in total

1.  Negative effect of cyclin D1 overexpression on recurrence-free survival in stage II-IIIA lung adenocarcinoma and its expression modulation by vorinostat in vitro.

Authors:  Eunju Lee; DongHao Jin; Bo Bin Lee; Yujin Kim; Joungho Han; Young Mog Shim; Duk-Hwan Kim
Journal:  BMC Cancer       Date:  2015-12-17       Impact factor: 4.430

Review 2.  HDAC inhibitors in kidney development and disease.

Authors:  Lauren L Brilli; Lisa M Swanhart; Mark P de Caestecker; Neil A Hukriede
Journal:  Pediatr Nephrol       Date:  2012-10-07       Impact factor: 3.714

3.  Correlation Analysis of Protein Expression of 10 HDAC/Sirtuin Isoenzymes with Sensitivities of 23 Anticancer Drugs in 17 Cancer Cell Lines and Potentiation of Drug Activity by Co-Treatment with HDAC Inhibitors.

Authors:  Steven Behnisch-Cornwell; Christoph W Grathwol; Lukas Schulig; Anika Voigt; Daniel Baecker; Andreas Link; Patrick J Bednarski
Journal:  Cancers (Basel)       Date:  2021-12-31       Impact factor: 6.639

4.  PinX1 suppresses bladder urothelial carcinoma cell proliferation via the inhibition of telomerase activity and p16/cyclin D1 pathway.

Authors:  Jian-Ye Liu; Dong Qian; Li-Ru He; Yong-Hong Li; Yi-Ji Liao; Shi-Juan Mai; Xiao-Peng Tian; Yan-Hui Liu; Jia-Xing Zhang; Hsiang-Fu Kung; Yi-Xin Zeng; Fang-Jian Zhou; Dan Xie
Journal:  Mol Cancer       Date:  2013-11-23       Impact factor: 27.401

5.  Hybrid topoisomerase I and HDAC inhibitors as dual action anticancer agents.

Authors:  Raffaella Cincinelli; Loana Musso; Roberto Artali; Mario B Guglielmi; Ilaria La Porta; Carmela Melito; Fabiana Colelli; Francesco Cardile; Giacomo Signorino; Alessandra Fucci; Martina Frusciante; Claudio Pisano; Sabrina Dallavalle
Journal:  PLoS One       Date:  2018-10-09       Impact factor: 3.240

  5 in total

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