Evidence map›Paper›PMID 39188277›Full record

ArticleSmart medicine2023

TP53 mutation-related senescence is an indicator of hepatocellular carcinoma patient outcomes from multiomics profiles.

Yu-Yan Chen, Zheng-Yi Zhu, Tao Ma, Lu Zhang, Jing Chen, Jia-Wei Jiang, Cui-Hua Lu, Yi-Tao Ding, Wen-Xian Guan, Nan Yi and 1 more

Abstract read
In one paragraph

Article in Smart medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

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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

3 citing papers in PubMed.

  1. 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

11 authors.

Yu-Yan ChenDepartment of Hepatobiliary Surgery Affiliated Drum Tower Hospital of Nanjing University Medical School Nanjing China.
Zheng-Yi ZhuDepartment of Hepatobiliary Surgery Affiliated Drum Tower Hospital of Nanjing University Medical School Nanjing China.
Tao MaDepartment of Gastroenterology Affiliated Hospital of Nantong University Nantong China.
Lu ZhangNanjing Drum Tower Hospital Clinical College of Jiangsu University Nanjing China.
Jing ChenDepartment of Gastroenterology Affiliated Hospital of Nantong University Nantong China.
Jia-Wei JiangDepartment of Gastroenterology Affiliated Hospital of Nantong University Nantong China.
Cui-Hua LuDepartment of Gastroenterology Affiliated Hospital of Nantong University Nantong China.
Yi-Tao DingDepartment of Hepatobiliary Surgery Affiliated Drum Tower Hospital of Nanjing University Medical School Nanjing China.
Wen-Xian GuanDepartment of General Surgery Affiliated Drum Tower Hospital of Nanjing University Medical School Nanjing China.
Nan YiDepartment of Gastroenterology Affiliated Hospital of Nantong University Nantong China.
Hao-Zhen RenDepartment of Hepatobiliary Surgery Affiliated Drum Tower Hospital of Nanjing University Medical School Nanjing China.ORCID https://orcid.org/0000-0002-6198-2904

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

TP53 mutation frequently occurs in hepatocellular carcinoma (HCC). Senescence also plays a vital role in the ongoing process of HCC. P53 is believed to regulate the advancement of senescence in HCC. However, the exact mechanism of TP53 mutation-related senescence remains unclear. In this study, we found the TP53 mutation was positively correlated with senescence in HCC, and the differential expressed genes were primarily located in macrophages. Our results proved that the risk score could have an independent and vital role in predicting the prognosis of HCC patients. In addition, HCC patients with a high risk score may most probably benefit from immune checkpoint block therapy. We also found the risk score is elevated in chemotherapy-treated HCC samples, with a high level of senescence-associated secretory phenotype. Finally, we validated the risk-score genes in the protein level and noticed the risk score is positively related with M2 polarization. Of note, we considered that the risk score under the TP53 mutation and senescence is a promising biomarker with the potential to aid in predicting prognosis, defining tumor environment characteristics, and assessing the benefits of immunotherapy for HCC patients.

Indexed as

hepatocellular carcinomaimmunotherapysenescencesenescence‐associated secretory phenotypeTP53 mutation

Identifiers

PMID39188277
PMCPMC11235654

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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.