Evidence map›Paper›PMID 27081081›Full record

ArticleOncotarget2016

Silencing homeobox C6 inhibits colorectal cancer cell proliferation.

Meiling Ji, Qingyang Feng, Guodong He, Liangliang Yang, Wentao Tang, Xinyuan Lao, Dexiang Zhu, Qi Lin, Pingping Xu, Ye Wei and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
5.7field-weighted citation impact, top 4% 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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 52 citations in OpenAlex.

  1. A Systematic Review onInternational journal of molecular sciences · 2021
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  11. Journal of Cancer · 2023
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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

11 authors at 4 institutions in 1 country.

Meiling JiDepartment of General Surgery, Zhongshan Hospital, Fudan University, Shanghai, China.
Qingyang FengDepartment of General Surgery, Zhongshan Hospital, Fudan University, Shanghai, China.
Guodong HeDepartment of General Surgery, Zhongshan Hospital, Fudan University, Shanghai, China.
Liangliang YangDepartment of General Surgery, Zhongshan Hospital, Fudan University, Shanghai, China.
Wentao TangDepartment of General Surgery, Zhongshan Hospital, Fudan University, Shanghai, China.
Xinyuan LaoDepartment of General Surgery, Zhongshan Hospital, Fudan University, Shanghai, China.
Dexiang ZhuDepartment of General Surgery, Zhongshan Hospital, Fudan University, Shanghai, China.
Qi LinDepartment of General Surgery, Zhongshan Hospital, Fudan University, Shanghai, China.
Pingping XuDepartment of General Surgery, Zhongshan Hospital, Fudan University, Shanghai, China.
Ye WeiDepartment of General Surgery, Zhongshan Hospital, Fudan University, Shanghai, China.
Jianmin XuDepartment of General Surgery, Zhongshan Hospital, Fudan University, Shanghai, China.
Fudan University · CNSun Yat-sen University · CNThe First Affiliated Hospital, Sun Yat-sen University · CNZhongshan Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Homeobox C6 (HOXC6), a member of the homeobox family that encodes highly conserved transcription factors, plays a vital role in various carcinomas. In this study, we used a tissue microarray (TMA) consisting of 462 CRC samples to demonstrate that HOXC6 is more abundantly expressed in colorectal cancer (CRC) tissues than adjacent normal mucosa. Clinicopathological data indicated that higher HOXC6 expression correlated with poor overall survival and was associated with primary tumor location in the right colon, primary tumor (pT) stage 3/4 and primary node (pN) stage 1/2. Multivariate analysis showed that high HOXC6 expression was an independent risk factor for poor CRC patient prognosis. HOXC6 downregulation via lentivirus-mediated expression of HOXC6-targeting shRNA reduced HCT116 cell viability and colony formation in vitro, and reduced growth of subcutaneous xenografts in nude mouse. HOXC6 thus appears to promote CRC cell proliferation and tumorigenesis through autophagy inhibition and mTOR pathway activation.

Indexed as

AdultAgedAnimalsAutophagyBiomarkers, TumorCell ProliferationCell Transformation, NeoplasticColorectal NeoplasmsFemaleGene Knockdown TechniquesHCT116 CellsHeterograftsHomeodomain ProteinsHumansKaplan-Meier EstimateMaleBiomarkers, TumorHomeodomain ProteinsHOXC6 protein, humanautophagycolorectal cancerHOXC6mTORproliferation

Identifiers

PMID27081081
PMCPMC5045391
OpenAlexW2337015381

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.