Evidence map›Paper›PMID 26885445›Full record

ArticleAmerican journal of cancer research2015

Volasertib suppresses tumor growth and potentiates the activity of cisplatin in cervical cancer.

Feng-Feng Xie, Shi-Shi Pan, Rong-Ying Ou, Zhen-Zhen Zheng, Xiao-Xiu Huang, Meng-Ting Jian, Jian-Ge Qiu, Wen-Ji Zhang, Qi-Wei Jiang, Yang Yang and 3 more

Abstract read
In one paragraph

Article in American journal of cancer research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed.

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  12. YM155 enhances docetaxel efficacy in ovarian cancer.American journal of translational research · 2018
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Feng-Feng XieDepartment of Gynecology, The First Affiliated Hospital of Wenzhou Medical University Wenzhou 325000, Zhejiang, China.
Shi-Shi PanDepartment of Gynecology, The First Affiliated Hospital of Wenzhou Medical University Wenzhou 325000, Zhejiang, China.
Rong-Ying OuDepartment of Gynecology, The First Affiliated Hospital of Wenzhou Medical University Wenzhou 325000, Zhejiang, China.
Zhen-Zhen ZhengDepartment of Gynecology, The First Affiliated Hospital of Wenzhou Medical University Wenzhou 325000, Zhejiang, China.
Xiao-Xiu HuangDepartment of Gynecology, The First Affiliated Hospital of Wenzhou Medical University Wenzhou 325000, Zhejiang, China.
Meng-Ting JianDepartment of Gynecology, The First Affiliated Hospital of Wenzhou Medical University Wenzhou 325000, Zhejiang, China.
Jian-Ge QiuDepartment of Cell Biology & Institute of Biomedicine, National Engineering Research Center of Genetic Medicine, Guangdong Provincial Key Laboratory of Bioengineering Medicine, College of Life Science and Technology, Jinan University Guangzhou 510632, Guangdong, China.
Wen-Ji ZhangDepartment of Cell Biology & Institute of Biomedicine, National Engineering Research Center of Genetic Medicine, Guangdong Provincial Key Laboratory of Bioengineering Medicine, College of Life Science and Technology, Jinan University Guangzhou 510632, Guangdong, China.
Qi-Wei JiangDepartment of Cell Biology & Institute of Biomedicine, National Engineering Research Center of Genetic Medicine, Guangdong Provincial Key Laboratory of Bioengineering Medicine, College of Life Science and Technology, Jinan University Guangzhou 510632, Guangdong, China.
Yang YangDepartment of Cell Biology & Institute of Biomedicine, National Engineering Research Center of Genetic Medicine, Guangdong Provincial Key Laboratory of Bioengineering Medicine, College of Life Science and Technology, Jinan University Guangzhou 510632, Guangdong, China.
Wen-Feng LiDepartment of Chemoradiotherpay, The First Affiliated Hospital of Wenzhou Medical University Wenzhou 325000, Zhejiang, China.
Zhi ShiDepartment of Cell Biology & Institute of Biomedicine, National Engineering Research Center of Genetic Medicine, Guangdong Provincial Key Laboratory of Bioengineering Medicine, College of Life Science and Technology, Jinan University Guangzhou 510632, Guangdong, China.
Xiao-Jian YanDepartment of Gynecology, The First Affiliated Hospital of Wenzhou Medical University Wenzhou 325000, Zhejiang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Volasertib (BI 6727), a highly selective and potent inhibitor of PLK1, has shown broad antitumor activities in the preclinical and clinical studies for the treatment of several types of cancers. However, the anticancer effect of volasertib on cervical cancer cells is still unknown. In the present study, we show that volasertib can markedly induce cell growth inhibition, cell cycle arrest at G2/M phase and apoptosis with the decreased protein expressions of PLK1 substrates survivin and wee1 in human cervical cancer cells. Furthermore, volasertib also enhances the intracellular reactive oxidative species (ROS) levels, and pretreated with ROS scavenger N-acety-L-cysteine totally blocks ROS generation but partly reverses volasertib-induced apoptosis. In addition, volasertib significantly potentiates the activity of cisplatin to inhibit the growth of cervical cancer in vitro and in vivo. In brief, volasertib suppresses tumor growth and potentiates the activity of cisplatin in cervical cancer, suggesting the combination of volasertib and cisplatin may be a promising strategy for the treatment of patients with cervical cancer.

Indexed as

cervical cancercisplatincombination therapyVolasertib

Identifiers

PMID26885445
PMCPMC4731630

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.