Evidence map›Paper›PMID 35958281›Full record

ArticleDisease markers2022

Pan-Cancer Analysis of Voltage-Dependent Anion Channel (VDAC1) as a Cancer Therapeutic Target or Diagnostic Biomarker.

Zhitong Wang, Yinchu Cheng, Zaiwei Song, Rongsheng Zhao

Open access · hybridAbstract read
In one paragraph

Article in Disease markers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

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  5. Oleanolic acid enhanced the anticancer effect of fluorouracil by regulating Ca2+ levels in hepatocellular carcinoma cells.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2025
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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

4 authors at 1 institution in 1 country.

Zhitong WangDepartment of Pharmacy, Peking University Third Hospital; Institute for Drug Evaluation, Peking University Health Science Center; Therapeutic Drug Monitoring and Clinical Toxicology Center, Peking University, Beijing 100191, China.ORCID https://orcid.org/0000-0001-9166-1047
Yinchu ChengDepartment of Pharmacy, Peking University Third Hospital; Institute for Drug Evaluation, Peking University Health Science Center; Therapeutic Drug Monitoring and Clinical Toxicology Center, Peking University, Beijing 100191, China.ORCID https://orcid.org/0000-0001-6084-0384
Zaiwei SongDepartment of Pharmacy, Peking University Third Hospital; Institute for Drug Evaluation, Peking University Health Science Center; Therapeutic Drug Monitoring and Clinical Toxicology Center, Peking University, Beijing 100191, China.ORCID https://orcid.org/0000-0001-7064-4459
Rongsheng ZhaoDepartment of Pharmacy, Peking University Third Hospital; Institute for Drug Evaluation, Peking University Health Science Center; Therapeutic Drug Monitoring and Clinical Toxicology Center, Peking University, Beijing 100191, China.ORCID https://orcid.org/0000-0002-3266-3496
Peking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The voltage-dependent anion channel 1 (VDAC1), a pore protein located in the outer mitochondrial membrane, has been confirmed to be related to cancer in cell or animal evidence. However, there is no available pan-cancer analysis of VDAC1. Herein, we investigated the potential roles of VDAC1 in tumorigenesis and progression based on the Cancer Genome Atlas (TCGA), Gene Expression Omnibus (GEO), and Clinical Proteomic Tumor Analysis Consortium (CPTAC) datasets. The expression of VDAC1 increased in most cancers, and the upregulation of VDAC1 distinctly correlated with the poor prognosis in patients, including breast invasive carcinoma, cervical squamous cell carcinoma, pancreatic adenocarcinoma, lung adenocarcinoma, and skin cutaneous melanoma. We also found VDAC1 S104 phosphorylation raised in various cancers, such as breast cancer, colon cancer, and lung adenocarcinoma. Moreover, the expression of VDAC1 was related to the estimated infiltration value of cancer-associated fibroblasts in bladder urothelial carcinoma, colon adenocarcinoma, kidney renal papillary cell carcinoma, and testicular germ cell tumors. At last, we showed that VDAC1-related oxidative phosphorylation and metabolic regulation may partially explain its association with tumorigenesis and progression. Taken together, this pan-cancer analysis provides relatively comprehensive information on the potential value of VDAC1 as a prognostic biomarker and therapeutic target.

Indexed as

AdenocarcinomaCarcinoma, Transitional CellColonic NeoplasmsMelanomaPancreatic NeoplasmsSkin NeoplasmsUrinary Bladder NeoplasmsAnimalsBiomarkersCarcinogenesisCutaneous Malignant MelanomaProteomicsVoltage-Dependent Anion ChannelsBiomarkersVoltage-Dependent Anion Channels

Identifiers

PMID35958281
PMCPMC9357804
OpenAlexW4289131850

What OpenQuestion holds

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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.