Evidence map›Paper›PMID 36176287›Full record

ArticleFrontiers in genetics2022

Cuproptosis patterns and tumor immune infiltration characterization in colorectal cancer.

Yan Du, Yilin Lin, Bo Wang, Yang Li, Duo Xu, Lin Gan, Xiaoyu Xiong, Sen Hou, Shuang Chen, Zhanlong Shen and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 8% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
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  10. Mechanisms of cuproptosis and its relevance to distinct diseases.Apoptosis : an international journal on programmed cell death · 2024
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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 at 2 institutions in 1 country.

Yan DuDepartment of Gastroenterological Surgery, Peking University People's Hospital, Beijing, China.
Yilin LinDepartment of Gastroenterological Surgery, Peking University People's Hospital, Beijing, China.
Bo WangDepartment of Gastroenterological Surgery, Peking University People's Hospital, Beijing, China.
Yang LiDepartment of Gastroenterological Surgery, Peking University People's Hospital, Beijing, China.
Duo XuDepartment of Gastroenterological Surgery, Peking University People's Hospital, Beijing, China.
Lin GanDepartment of Gastroenterological Surgery, Peking University People's Hospital, Beijing, China.
Xiaoyu XiongDepartment of Gastroenterological Surgery, Peking University People's Hospital, Beijing, China.
Sen HouDepartment of Gastroenterological Surgery, Peking University People's Hospital, Beijing, China.
Shuang ChenDepartment of Gastroenterological Surgery, Peking University People's Hospital, Beijing, China.
Zhanlong ShenDepartment of Gastroenterological Surgery, Peking University People's Hospital, Beijing, China.
Yingjiang YeDepartment of Gastroenterological Surgery, Peking University People's Hospital, Beijing, China.
Peking University · CNPeking University People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Faced with the high heterogeneity and poor prognosis of colorectal cancer (CRC), this study sought to find new predictive prognostic strategies to improve the situation. Cuproptosis is a novel cell death mechanism that relies on copper regulation. However, the role of cuproptosis-related gene (CRG) in CRC remains to be elucidated. In this study, we comprehensively assessed the CRG landscape in CRC based on The Cancer Genome Atlas (TCGA). We identified differential expression and genetic alterations of CRG in CRC. CRG is highly correlated with initiation, progression, prognosis, and immune infiltration of CRC. We construct a risk score signature containing 3 CRGs based on LASSO. We explored the correlation of CRG-Score with clinicopathological features of CRC. Age, stage, and CRG-Score were integrated to construct a nomogram. The nomogram has robust predictive performance. We also understand the correlation of CRG-Score with CRC immune landscape. CRG-Score can effectively predict the immune landscape of CRC patients. Low-risk CRC patients have greater immunogenicity and higher immune checkpoint expression. Low-risk CRC patients may be better candidates for immunotherapy. At the same time, we also predicted more sensitive drugs in the high-risk CRC patients. In conclusion, the CRG risk score signature is a strong prognostic marker and may help provide new insights into the treatment of individuals with CRC.

Indexed as

CRCcuproptosisgene signatureimmune statusoverall survival

Identifiers

PMID36176287
PMCPMC9513614
OpenAlexW4297888397

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.