Evidence map›Paper›PMID 25120779›Full record

ArticleInternational journal of clinical and experimental pathology2014

Cyclin D1b overexpression inhibits cell proliferation and induces cell apoptosis in cervical cancer cells in vitro and in vivo.

Ning Wang, Heng Wei, Duo Yin, Yanming Lu, Yao Zhang, Di Jiang, Yan Jiang, Shulan Zhang

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-weighted citation impact, top 32% of its field
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

9 citing papers in PubMed, 12 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Ning WangDepartment of Obstetrics and Gynecology, Shengjing Hospital of China Medical University Shenyang 110004, People's Republic of China.
Heng WeiDepartment of Obstetrics and Gynecology, Shengjing Hospital of China Medical University Shenyang 110004, People's Republic of China.
Duo YinDepartment of Obstetrics and Gynecology, Shengjing Hospital of China Medical University Shenyang 110004, People's Republic of China.
Yanming LuDepartment of Obstetrics and Gynecology, Shengjing Hospital of China Medical University Shenyang 110004, People's Republic of China.
Yao ZhangDepartment of Obstetrics and Gynecology, Shengjing Hospital of China Medical University Shenyang 110004, People's Republic of China.
Di JiangDepartment of Obstetrics and Gynecology, Shengjing Hospital of China Medical University Shenyang 110004, People's Republic of China.
Yan JiangDepartment of Obstetrics and Gynecology, Shengjing Hospital of China Medical University Shenyang 110004, People's Republic of China.
Shulan ZhangDepartment of Obstetrics and Gynecology, Shengjing Hospital of China Medical University Shenyang 110004, People's Republic of China.
China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cyclin D1b is one of two proteins translated from cyclin D1 transcripts (isoforms a and b) that are generated due to gene polymorphism. Our previous study has reported low cyclin D1b expression in cervical cancer tissue, with an expression level in moderately or poorly differentiated tissues that was significantly lower than that in well-differentiated tissues. However, the functional role of cyclin D1b in cervical cancer remains to be elucidated. In this study, using a cervical cancer cell line with stable expression of cyclin D1b, we found that upregulation of cyclin D1b initiated cell cycle arrest at the G0/G1 phase and induced apoptosis, thereby inhibiting cell proliferation and colony formation. Furthermore, xenograft transplantation experiments in nude mice demonstrated that cyclin D1b upregulation inhibited cancer growth and induce apoptosis in vivo. In conclusion, the present study indicates anti-tumor effects of cyclin D1b in cervical cancer, suggesting that cyclin D1b may represent a potential therapeutic target for cervical cancer.

Indexed as

AnimalsApoptosisBlotting, WesternCell ProliferationCyclin D1FemaleFlow CytometryHeLa CellsHeterograftsHumansIn Situ Nick-End LabelingIn Vitro TechniquesMiceMice, NudeProtein IsoformsReal-Time Polymerase Chain ReactionCyclin D1Protein Isoformsapoptosiscervical cancerCyclin D1bproliferation

Identifiers

PMID25120779
PMCPMC4129014
OpenAlexW221582945

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.