Literature DB >> 16054570

Clinical potential of inhibitors of survival pathways and activators of apoptotic pathways in treatment of cervical cancer: changing the apoptotic balance.

Brigitte M T Hougardy1, John H Maduro, Ate G J van der Zee, Pax H B Willemse, Steven de Jong, Elisabeth G E de Vries.   

Abstract

Cervical cancer is the most common gynaecological malignant disorder worldwide. The best possible treatment of locally advanced cervical cancer is a combination of radiation and cisplatin-based chemotherapy. However, 5-year overall survival is still only 52%. To improve treatment results, research should focus on the discovery of innovative drug strategies. Drugs directed at inducing tumour-cell apoptosis are regarded as important treatment modalities. Here, we present an overview of the molecular options that can change the apoptotic balance in cervical cancer, through increasing death-receptor-mediated apoptosis, the use of proteasome inhibitors, short interfering RNAs, or non-steroidal anti-inflammatory drugs (NSAIDs). Furthermore, the potential of attacking prosurvival signalling through the epidermal-growth-factor receptor and insulin-like-growth-factor receptor to support the apoptotic process is discussed. Additional research is needed to elucidate the clinical potential of these compounds in the treatment of cervical cancer.

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Year:  2005        PMID: 16054570     DOI: 10.1016/S1470-2045(05)70281-3

Source DB:  PubMed          Journal:  Lancet Oncol        ISSN: 1470-2045            Impact factor:   41.316


  14 in total

1.  Inhibitors of metabolism rescue cell death in Huntington's disease models.

Authors:  Hemant Varma; Richard Cheng; Cindy Voisine; Anne C Hart; Brent R Stockwell
Journal:  Proc Natl Acad Sci U S A       Date:  2007-08-28       Impact factor: 11.205

2.  Downregulation of Foxc2 enhances apoptosis induced by 5-fluorouracil through activation of MAPK and AKT pathways in colorectal cancer.

Authors:  Chao Yang; Xiaoxian Cui; Xiaoqin Dai; Wenting Liao
Journal:  Oncol Lett       Date:  2016-01-08       Impact factor: 2.967

3.  Knock down of p53 or its ubiquitin ligase E6AP does not affect the sensitivity of human papillomavirus-positive cervical cancer cells to cisplatin.

Authors:  Olga Michnov; Erich Solomayer; Tanja Fehm; Frank Stubenrauch; Thomas Iftner
Journal:  Am J Cancer Res       Date:  2012-04-22       Impact factor: 6.166

4.  Apoptotic potential role of Agave palmeri and Tulbaghia violacea extracts in cervical cancer cells.

Authors:  Nonkululeko N Mthembu; Lesetja Raymond Motadi
Journal:  Mol Biol Rep       Date:  2014-07-04       Impact factor: 2.316

5.  Regulation of cell growth through cell cycle arrest and apoptosis in HPV 16 positive human cervical cancer cells by tea polyphenols.

Authors:  Madhulika Singh; Shilpa Tyagi; Kulpreet Bhui; Sahdeo Prasad; Yogeshwer Shukla
Journal:  Invest New Drugs       Date:  2009-03-07       Impact factor: 3.850

6.  Correlating EGFR expression with receptor-binding properties and internalization of 64Cu-DOTA-cetuximab in 5 cervical cancer cell lines.

Authors:  Martin Eiblmaier; Laura A Meyer; Mark A Watson; Paula M Fracasso; Linda J Pike; Carolyn J Anderson
Journal:  J Nucl Med       Date:  2008-08-14       Impact factor: 10.057

7.  Melatonin increases human cervical cancer HeLa cells apoptosis induced by cisplatin via inhibition of JNK/Parkin/mitophagy axis.

Authors:  Li Chen; Liping Liu; Yinghui Li; Jing Gao
Journal:  In Vitro Cell Dev Biol Anim       Date:  2017-10-25       Impact factor: 2.416

8.  Enhanced killing of cervical cancer cells by combinations of methyl jasmonate with cisplatin, X or alpha radiation.

Authors:  Elad Milrot; Anna Jackman; Eliezer Flescher; Pinhas Gonen; Itzhak Kelson; Yona Keisari; Levana Sherman
Journal:  Invest New Drugs       Date:  2012-09-06       Impact factor: 3.850

9.  RIPK3 expression in cervical cancer cells is required for PolyIC-induced necroptosis, IL-1α release, and efficient paracrine dendritic cell activation.

Authors:  Susanne V Schmidt; Stefanie Seibert; Barbara Walch-Rückheim; Benjamin Vicinus; Eva-Maria Kamionka; Jennifer Pahne-Zeppenfeld; Erich-Franz Solomayer; Yoo-Jin Kim; Rainer M Bohle; Sigrun Smola
Journal:  Oncotarget       Date:  2015-04-20

10.  Nutlin-3 preferentially sensitises wild-type p53-expressing cancer cells to DR5-selective TRAIL over rhTRAIL.

Authors:  A Meijer; F A E Kruyt; A G J van der Zee; H Hollema; P Le; K A ten Hoor; G M M Groothuis; W J Quax; E G E de Vries; S de Jong
Journal:  Br J Cancer       Date:  2013-10-17       Impact factor: 7.640

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