Evidence map›Paper›PMID 26307391›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2016

HIF-2α regulates CDCP1 to promote PKCδ-mediated migration in hepatocellular carcinoma.

Manqing Cao, Junrong Gao, Hongyuan Zhou, Jiafei Huang, Abin You, Zhigui Guo, Feng Fang, Wei Zhang, Tianqiang Song, Ti Zhang

Abstract read
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In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

17 citing papers in PubMed, 26 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

10 authors at 2 institutions in 1 country.

Manqing CaoDepartment of Hepatobiliary Surgery, National Clinical Research Center for Cancer, Key laboratory of Cancer Prevention and Therapy, Tianjin Medical University Cancer Institute and Hospital, 24 Bin Shui Road, Hexi District, Tianjin, 300060, People's Republic of China.
Junrong GaoAcademy of Medical Image, Tianjin Medical University, Tianjin, People's Republic of China.
Hongyuan ZhouDepartment of Hepatobiliary Surgery, National Clinical Research Center for Cancer, Key laboratory of Cancer Prevention and Therapy, Tianjin Medical University Cancer Institute and Hospital, 24 Bin Shui Road, Hexi District, Tianjin, 300060, People's Republic of China.
Jiafei HuangDepartment of Hepatobiliary Surgery, National Clinical Research Center for Cancer, Key laboratory of Cancer Prevention and Therapy, Tianjin Medical University Cancer Institute and Hospital, 24 Bin Shui Road, Hexi District, Tianjin, 300060, People's Republic of China.
Abin YouDepartment of Hepatobiliary Surgery, National Clinical Research Center for Cancer, Key laboratory of Cancer Prevention and Therapy, Tianjin Medical University Cancer Institute and Hospital, 24 Bin Shui Road, Hexi District, Tianjin, 300060, People's Republic of China.
Zhigui GuoDepartment of Hepatobiliary Surgery, National Clinical Research Center for Cancer, Key laboratory of Cancer Prevention and Therapy, Tianjin Medical University Cancer Institute and Hospital, 24 Bin Shui Road, Hexi District, Tianjin, 300060, People's Republic of China.
Feng FangDepartment of Hepatobiliary Surgery, National Clinical Research Center for Cancer, Key laboratory of Cancer Prevention and Therapy, Tianjin Medical University Cancer Institute and Hospital, 24 Bin Shui Road, Hexi District, Tianjin, 300060, People's Republic of China.
Wei ZhangDepartment of Hepatobiliary Surgery, National Clinical Research Center for Cancer, Key laboratory of Cancer Prevention and Therapy, Tianjin Medical University Cancer Institute and Hospital, 24 Bin Shui Road, Hexi District, Tianjin, 300060, People's Republic of China.
Tianqiang SongDepartment of Hepatobiliary Surgery, National Clinical Research Center for Cancer, Key laboratory of Cancer Prevention and Therapy, Tianjin Medical University Cancer Institute and Hospital, 24 Bin Shui Road, Hexi District, Tianjin, 300060, People's Republic of China. tjchi@hotmail.com.
Ti ZhangDepartment of Hepatobiliary Surgery, National Clinical Research Center for Cancer, Key laboratory of Cancer Prevention and Therapy, Tianjin Medical University Cancer Institute and Hospital, 24 Bin Shui Road, Hexi District, Tianjin, 300060, People's Republic of China. zhangti@tjmuch.com.
Tianjin Medical University Cancer Institute and Hospital · CNTianjin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Overexpression of CUB domain-containing protein 1 (CDCP1), a transmembrane glycoprotein and major substrate of Src family kinases (SFKs), always indicates unfavorable outcomes in various cancers. The characteristics of CDCP1 in hepatocellular carcinoma (HCC) have not been assessed. Most recently, CDCP1 was identified as a specific target gene of HIF-2α in clear cell renal carcinoma (CC-RCC). However, considering the role of HIF-2α in the progression of HCC is highly controversial, it is necessary to figure out whether HIF-2α and CDCP1 play a significant part in the metastasis of HCC. Our results showed that HIF-2α and CDCP1 were both induced by hypoxia, and the activation of CDCP1 was HIF-2α dependent. CDCP1 was governed by HIF-2α at mRNA and protein levels in HCC cell lines. Moreover, knocking down of HIF-2α not only inhibited cell invasion but also impaired the expression of Tyr(311) phosphorylation of protein kinase Cδ (PKCδ) which is a downstream factor of CDCP1 and has been reported to induce malignant migration in various tumors. Analysis of human HCC samples showed a negative correlation of CDCP1 expression with disease-free survival, and CDCP1 was an independent prognostic factors of disease-free survival. Taken together, these data demonstrated that HIF-2α could promote HCC cell migration by regulating CDCP1, and targeting HIF-2α-CDCP1-PKCδ pathway might be effective to inhibit HCC metastasis.

Indexed as

AcetylcysteineAnimalsAntigens, CDAntigens, NeoplasmBasic Helix-Loop-Helix ProteinsBlotting, WesternCarcinoma, HepatocellularCell Adhesion MoleculesCell MovementEndothelial PAS Domain-Containing Protein 1Gene Expression Regulation, NeoplasticHeterograftsHumansImmunohistochemistryLiver NeoplasmsMiceAcetylcysteineAntigens, CDAntigens, NeoplasmBasic Helix-Loop-Helix ProteinsCDCP1 protein, humanCell Adhesion MoleculesEndothelial PAS Domain-Containing Protein 1Neoplasm ProteinsProtein Kinase C-deltaCDCP1Hepatocellular carcinomaHIF-2αMetastasisPKCδ

Identifiers

PMID26307391
OpenAlexW1184375026

What OpenQuestion holds

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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.