Literature DB >> 28285964

Survivin and gynaecological tumours.

Dušan Braný1, Dana Dvorská2, Pavol Slávik3, Richard Školka4, Marián Adamkov5.   

Abstract

Survivin is the smallest member of the inhibitors of apoptosis (IAP) family. However, participation in inhibition of apoptosis is not the only function of this molecule. Survivin can also affect the proper process of mitosis and even promoting of angiogenesis or DNA repair. High levels of survivin expression are connected with foetal tissues during intrauterine development. In the overwhelming majority of healthy, differentiated adult tissues, amounts of survivin are markedly reduced. On the other hand, survivin is also often abundantly expressed in cases of various types of cancer. Generally, high expression levels of survivin are associated with a poor prognosis, an increased rate of tumour recurrence and high resistance to chemo- as well as radiotherapy, hence survivin can be considered a factor in the initiation and progression of many types of cancer with great significance and potential for cancer therapy. Nonetheless, progress in development of survivin inhibitors or primarily, in survivin-related molecular therapies, is surprisingly not very fast and indeed remains a challenge for the future. The objective of this article is to summarize known facts about survivin, its contribution to inhibition of apoptosis and cell division and its implication in the development of gynaecological tumours. At the end, known survivin inhibitors and their effect on regulation of tumour growth will be referenced.
Copyright © 2017 Elsevier GmbH. All rights reserved.

Entities:  

Keywords:  Apoptosis; BIRC5; Cell death; Gynaecological tumours; Survivin

Mesh:

Substances:

Year:  2017        PMID: 28285964     DOI: 10.1016/j.prp.2017.02.009

Source DB:  PubMed          Journal:  Pathol Res Pract        ISSN: 0344-0338            Impact factor:   3.250


  7 in total

1.  Integration of multiple networks and pathways identifies cancer driver genes in pan-cancer analysis.

Authors:  Claudia Cava; Gloria Bertoli; Antonio Colaprico; Catharina Olsen; Gianluca Bontempi; Isabella Castiglioni
Journal:  BMC Genomics       Date:  2018-01-06       Impact factor: 3.969

2.  miR-596 suppresses the expression of Survivin and enhances the sensitivity of osteosarcoma cells to the molecular targeting agent anlotinib.

Authors:  Leisheng Wang; He En; Lei Yang; Yanbing Zhang; Baisheng Sun; Jianjiang Gao
Journal:  Onco Targets Ther       Date:  2019-08-21       Impact factor: 4.147

3.  Effects of ginsenoside Rb1 on spinal cord ischemia-reperfusion injury in rats.

Authors:  Jin-Tao Ye; Feng-Tao Li; Sheng-Li Huang; Jian-Li Xue; Yirixiati Aihaiti; Hao Wu; Ruo-Xi Liu; Bin Cheng
Journal:  J Orthop Surg Res       Date:  2019-08-14       Impact factor: 2.359

4.  Survivin Promotes Piperlongumine Resistance in Ovarian Cancer.

Authors:  Xing-Wei Nan; Li-Hua Gong; Xu Chen; Hai-Hong Zhou; Piao-Piao Ye; Yang Yang; Zi-Hao Xing; Meng-Ning Wei; Yao Li; Sheng-Te Wang; Kun Liu; Zhi Shi; Xiao-Jian Yan
Journal:  Front Oncol       Date:  2019-11-29       Impact factor: 6.244

5.  Targeting abundant survivin expression in liposarcoma: subtype dependent therapy responses to YM155 treatment.

Authors:  Christian Vay; Philipp M Schlünder; Levent Dizdar; Irene Esposito; Markus P H Ghadimi; Wolfram T Knoefel; Andreas Krieg
Journal:  J Cancer Res Clin Oncol       Date:  2021-12-03       Impact factor: 4.322

6.  Clinicopathological and Prognostic Value of Survivin Expression in Surgically Resected Pancreatic Ductal Adenocarcinoma.

Authors:  Christian Vay; Shahrooz Babaei; Sami-Alexander Safi; Levent Dizdar; Alexander Rehders; Lena Haeberle; Christoph Roderburg; Sven H Loosen; Irene Esposito; Wolfram T Knoefel; Andreas Krieg
Journal:  Cancers (Basel)       Date:  2022-07-18       Impact factor: 6.575

Review 7.  Survivin-Based Treatment Strategies for Squamous Cell Carcinoma.

Authors:  Andrea Santarelli; Marco Mascitti; Lucio Lo Russo; Davide Sartini; Giuseppe Troiano; Monica Emanuelli; Lorenzo Lo Muzio
Journal:  Int J Mol Sci       Date:  2018-03-24       Impact factor: 5.923

  7 in total

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