Evidence map›Paper›PMID 26312564›Full record

ArticleOncotarget2015

CCDC34 is up-regulated in bladder cancer and regulates bladder cancer cell proliferation, apoptosis and migration.

Yanqing Gong, Wei Qiu, Xianghui Ning, Xinyu Yang, Libo Liu, Zicheng Wang, Jian Lin, Xuesong Li, Yinglu Guo

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

36 citing papers in PubMed, 45 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

9 authors at 3 institutions in 1 country.

Yanqing GongDepartment of Urology, Peking University First Hospital, Beijing 100034, China.
Wei QiuDepartment of Urology, Beijing Friendship Hospital, Capital Medical University, Beijing 100050, China.
Xianghui NingDepartment of Urology, Peking University First Hospital, Beijing 100034, China.
Xinyu YangDepartment of Urology, Peking University First Hospital, Beijing 100034, China.
Libo LiuDepartment of Urology, Peking University First Hospital, Beijing 100034, China.
Zicheng WangDepartment of Urology, Peking University First Hospital, Beijing 100034, China.
Jian LinDepartment of Urology, Peking University First Hospital, Beijing 100034, China.
Xuesong LiDepartment of Urology, Peking University First Hospital, Beijing 100034, China.
Yinglu GuoDepartment of Urology, Peking University First Hospital, Beijing 100034, China.
Peking University First Hospital · CNPeking University · CNBeijing Friendship Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The coiled coil is a superhelical structural protein motif involved in a diverse array of biological functions, and the abnormal expression of the coiled-coil domain containing proteins has a direct link with the phenotype of tumor cell migration, invasion and metastasis. The aim of this study was to investigate the critical role of Coiled-coil domain-containing protein 34 (CCDC34) in bladder carcinogenesis, which has never been reported to date. Here, we found CCDC34 expression was elevated in bladder cancer tissues and cell lines. The knockdown of CCDC34 via lentivirus-mediated siRNA significantly suppressed bladder cancer cells proliferation and migration, and induced cell cycle arrest at G2/M phase and increased apoptosis in vitro. In addition, CCDC34 knockdown suppressed bladder tumor growth in nude mice. Moreover, CCDC34 silencing decreased the phosphorylation of MEK, ERK1/2, JNK, p38 and Akt, and the expressions of c-Raf and c-Jun, indicating MAPK and AKT pathways (ERK/MAPK, p38/MAPK, JNK/MAPK and PI3K/Akt) might be involved in CCDC34 regulation of bladder cancer cell proliferation and migration. Our findings revealed for the first time a potential oncogenic role for CCDC34 in bladder carcinoma pathogenesis and it may serve as a biomarker or even a therapeutic target for bladder cancer.

Indexed as

ApoptosisCell MovementCell ProliferationAdultAgedAged, 80 and overAnimalsAntigens, NeoplasmCell Line, TumorEnzyme ActivationFemaleG2 Phase Cell Cycle CheckpointsGene Expression Regulation, NeoplasticHumansMaleMice, Inbred BALB CAntigens, NeoplasmCCDC34 protein, humanMitogen-Activated Protein KinasesNeoplasm ProteinsProto-Oncogene Proteins c-aktbladder cancerCCDC34migrationproliferationsiRNA

Identifiers

PMID26312564
PMCPMC4694871
OpenAlexW2146479736

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.