Evidence map›Paper›PMID 36158487›Full record

ArticleWorld journal of clinical cases2022

Comprehensive proteomic signature and identification of CDKN2A as a promising prognostic biomarker and therapeutic target of colorectal cancer.

Qian-Qian Wang, Yuan-Chen Zhou, Yu-Jia Zhou Ge, Geng Qin, Teng-Fei Yin, Dong-Yan Zhao, Chang Tan, Shu-Kun Yao

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Article in World journal of clinical cases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

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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

13 citing papers in PubMed.

  1. Review
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  12. Colorectal Cancer: From Risk Factors to Oncogenesis.Medicina (Kaunas, Lithuania) · 2023
    Review
  13. Article
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

8 authors.

Qian-Qian WangGraduate School, Peking University China-Japan Friendship School of Clinical Medicine, Beijing 10029, China.
Yuan-Chen ZhouGraduate School, Peking University China-Japan Friendship School of Clinical Medicine, Beijing 10029, China.
Yu-Jia Zhou GeGraduate School, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100730, China.
Geng QinDepartment of Gastroenterology, China-Japan Friendship Hospital, Beijing 100029, China.
Teng-Fei YinGraduate School, Peking University China-Japan Friendship School of Clinical Medicine, Beijing 100029, China.
Dong-Yan ZhaoGraduate School, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100730, China.
Chang TanGraduate School, Peking University China-Japan Friendship School of Clinical Medicine, Beijing 100029, China.
Shu-Kun YaoDepartment of Gastroenterology, China-Japan Friendship Hospital, Beijing 100029, China. shukunyao@126.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe carcinogenesis of colorectal cancer (CRC) involves many different molecules and multiple pathways, and the specific mechanism has not been elucidated until now. Existing studies on the proteomic signature profiles of CRC are relatively limited. Therefore, we herein aimed to provide a more comprehensive proteomic signature profile and discover new prognostic markers and therapeutic targets by performing proteomic analysis of CRC and paired normal tissues.

aimTo investigate the proteomic signature and identify novel protein prognostic biomarkers of CRC.

methodsCancer tissues and paired normal tissues were collected from 48 patients who underwent surgical removal at the China-Japan Friendship Hospital from January 2020 to June 2021. Data independent acquisition (DIA) quantitative proteomic analysis was performed using high-performance liquid chromatography-mass spectrometry/mass spectrometry (nano-UHPLC-MS/MS) to identify differentially expressed proteins, among which those with a

resultsSignificantly differential protein expression was observed between cancer tissues and normal tissues. Compared with normal tissues, 1115 proteins were upregulated and 705 proteins were downregulated in CRC based on

conclusionOur study provides a comprehensive proteomic signature of CRC and highlights CDKN2A as a potential powerful prognostic marker and precision therapeutic target.

Indexed as

Colorectal cancerCyclin-dependent kinase inhibitor 2APrecision treatmentPrognostic biomarkerProteomic analysisTherapeutic target

Identifiers

PMID36158487
PMCPMC9372836

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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.