Evidence map›Paper›PMID 35414774›Full record

ArticleInternational journal of biological sciences2022

Mutant p53 achieved Gain-of-Function by promoting tumor growth and immune escape through PHLPP2/AKT/PD-L1 pathway.

Nannan Liu, Xinxiu Jiang, Leiming Guo, Chuchu Zhang, Meimei Jiang, Zhuoran Sun, Yizheng Zhang, Wunan Mi, Jiehan Li, Yang Fu and 3 more

Open access · goldAbstract read
In one paragraph

Article in International journal of biological sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.1field-weighted citation impact, top 11% 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

23 citing papers in PubMed, 22 citations in OpenAlex.

  1. Mutant p53Molecular oncology · 2026
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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

13 authors at 4 institutions in 1 country.

Nannan LiuSchool of Biomedical Sciences, Hunan University, Changsha, China.
Xinxiu JiangSchool of Biomedical Sciences, Hunan University, Changsha, China.
Leiming GuoDepartment of Gastroenterology, Huadong Hospital, Shanghai Medical College, Fudan University, Shanghai, China.
Chuchu ZhangSchool of Biomedical Sciences, Hunan University, Changsha, China.
Meimei JiangSchool of Biomedical Sciences, Hunan University, Changsha, China.
Zhuoran SunDepartment of Laboratory Medicine, the Third Xiangya Hospital, Central South University, Changsha, China.
Yizheng ZhangSchool of Biomedical Sciences, Hunan University, Changsha, China.
Wunan MiSchool of Biomedical Sciences, Hunan University, Changsha, China.
Jiehan LiSchool of Biomedical Sciences, Hunan University, Changsha, China.
Yang FuDepartment of Gastroenterology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, China.
Feng WangDepartment of Gastroenterology, Huadong Hospital, Shanghai Medical College, Fudan University, Shanghai, China.
Lingling ZhangDepartment of Laboratory Medicine, the Third Xiangya Hospital, Central South University, Changsha, China.
Yingjie ZhangSchool of Biomedical Sciences, Hunan University, Changsha, China.
Hunan University · CNFirst Affiliated Hospital of Zhengzhou University · CNHuadong Hospital · CNThird Xiangya Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The most frequent genetic alterations of the TP53 gene in human cancer were reported. TP53 mutation gains new function as a target of genetic instability, which is associated with increased tumor progression and poor survival rate in patients. In this study, more than three hundred colorectal cancer patients' samples were firstly analyzed, and the results showed that patients with mutant p53 had higher levels of AKT phosphorylation and PD-L1 expression, which were next verified both in cell lines

Indexed as

B7-H1 AntigenProto-Oncogene Proteins c-aktCell Line, TumorGain of Function MutationGenes, p53HumansPhosphoprotein PhosphatasesTumor Suppressor Protein p53B7-H1 AntigenCD274 protein, humanPHLPP2 protein, humanPhosphoprotein PhosphatasesProto-Oncogene Proteins c-aktTP53 protein, humanTumor Suppressor Protein p53AKTimmunitymutant TP53PD-L1PHLPP2

Identifiers

PMID35414774
PMCPMC8990467
OpenAlexW4226033466

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.