Evidence map›Paper›PMID 35314790›Full record

ArticleOncogene2022

The proteomic characterization of the peritumor microenvironment in human hepatocellular carcinoma.

Yuhan Gu, Yuanyuan Guo, Na Gao, Yan Fang, Chen Xu, Guiming Hu, Mengxue Guo, Yaxing Ma, Yunfei Zhang, Jun Zhou and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Oncogene, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
5.2field-weighted citation impact, top 3% 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

22 citing papers in PubMed, 47 citations in OpenAlex.

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  18. New and Old Key Players in Liver Cancer.International journal of molecular sciences · 2023
    Review
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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

14 authors at 1 institution in 1 country.

Yuhan Gu *Institute of Clinical Pharmacology, Zhengzhou University, Zhengzhou, China.
Yuanyuan Guo *Institute of Clinical Pharmacology, Zhengzhou University, Zhengzhou, China.
Na Gao *Institute of Clinical Pharmacology, Zhengzhou University, Zhengzhou, China.
Yan Fang *Institute of Clinical Pharmacology, Zhengzhou University, Zhengzhou, China.
Chen XuInstitute of Clinical Pharmacology, Zhengzhou University, Zhengzhou, China.
Guiming HuInstitute of Clinical Pharmacology, Zhengzhou University, Zhengzhou, China.
Mengxue GuoInstitute of Clinical Pharmacology, Zhengzhou University, Zhengzhou, China.
Yaxing MaInstitute of Clinical Pharmacology, Zhengzhou University, Zhengzhou, China.
Yunfei ZhangAffiliated Cancer Hospital of Zhengzhou University, Zhengzhou, China.
Jun ZhouAffiliated People's Hospital of Zhengzhou University, Zhengzhou, China.
Yanlin LuoAffiliated Cancer Hospital of Zhengzhou University, Zhengzhou, China.
Haifeng ZhangInstitute of Clinical Pharmacology, Zhengzhou University, Zhengzhou, China.
Qiang WenInstitute of Clinical Pharmacology, Zhengzhou University, Zhengzhou, China.
Hailing QiaoInstitute of Clinical Pharmacology, Zhengzhou University, Zhengzhou, China. qiaohl@zzu.edu.cn.ORCID http://orcid.org/0000-0002-8533-344X
Zhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The tumor microenvironment (TME) was usually studied in tumor tissue and in relation to only tumor progression, with little involved in occurrence, recurrence and metastasis of tumor. Thus, a new concept "peritumor microenvironment (PME)" was proposed in the proteomic characterization of peritumor liver tissues in human hepatocellular carcinoma (HCC). The PME for occurrence (PME-O) and progression (PME-P) were almost totally different at proteome composition and function. Proteins for occurrence and progression rarely overlapped and crossed. Immunity played a central role in PME-O, whereas inflammation, angiogenesis and metabolism were critical in PME-P. Proteome profiling identified three PME subtypes with different features of HCC. Thymidine phosphorylase (TYMP) was validated as an antiangiogenic target in an orthotopic HCC mouse model. Overall, the proteomic characterization of the PME revealed that the entire processes of HCC occurrence and progression differ substantially. These findings could enable advances in cancer biology, diagnostics and therapeutics.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsAnimalsHumansMiceProteomeProteomicsTumor MicroenvironmentProteome

Identifiers

PMID35314790
PMCPMC9033583
OpenAlexW4221071191

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.