Evidence map›Paper›PMID 42266181›Full record

ArticleMedComm2026

Integrative Proteogenomic Characterization of Left-Sided and Right-Sided Colorectal Cancer.

An Huang, Haopeng Hong, Yonghui Sun, Zhaoya Gao, Jingxuan Xu, Jiajia Chen, Yong Yang, Zhongyi Chen, Hebing Chen, Ming Li and 2 more

Abstract read
In one paragraph

Article in MedComm, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

An HuangDepartment of General Surgery, The First Affiliated Hospital, Jiangxi Medical College Nanchang University Nanchang Jiangxi China.
Haopeng HongDepartment of General Surgery Peking University First Hospital Beijing China.
Yonghui SunThe Second Clinical Medical College Xinjiang Medical University Urumqi China.
Zhaoya GaoDepartment of Gastrointestinal Surgery Peking University Shougang Hospital Beijing China.
Jingxuan XuDepartment of Radiotherapy Peking University Shougang Hospital Beijing China.
Jiajia ChenDepartment of Gastrointestinal Surgery Peking University Shougang Hospital Beijing China.
Yong YangDepartment of Gastrointestinal Surgery Peking University Shougang Hospital Beijing China.
Zhongyi ChenJingjie PTM BioLab Co. Ltd. Hangzhou China.
Hebing ChenAcademy of Military Medical Science Beijing China.
Ming LiDepartment of Gastrointestinal Surgery Peking University Shougang Hospital Beijing China.
Xiaodong WangDepartment of Oncology Peking University Shougang Hospital Beijing China.
Jin GuThe Second Clinical Medical College Xinjiang Medical University Urumqi China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Distinguishing characteristics have been found in the left-sided and right-sided colorectal cancer (CRC), which have different embryonic origins, molecular and clinical features. These result in differences in the efficacy of targeted therapy and immunotherapy. Multi-omics characterization, predicated upon tumor laterality, may facilitate a more precise and personalized approach to the treatment of patients with CRC. Encompassing whole-exome, proteomics, and phosphoproteomics sequencing, we conducted a comprehensive investigation of tumor and matched normal adjacent tissues from a total of 80 pairs of patients with CRC. Results revealed that the pathogenesis of left-sided CRC was predominantly associated with chromosomal instability, while right-sided CRC was primarily linked to microsatellite instability. Regarding the tumor microenvironment, left-sided CRC exhibited predominant microvascular endothelial cell proliferation, while right-sided CRC displayed enhanced MHC Class II-associated antigen presentation mediated by M1 macrophages. Additionally, the proportion of deficient mismatch repair that developed into microsatellite instability-high was observed to be lower in the left-sided CRC compared to the right-sided, indicating divergent DNA damage repair systems between laterality subtypes that contribute to differential immunotherapy efficacy. This integrated proteogenomic study provides a comprehensive and nuanced understanding of the molecular heterogeneity between left- and right-sided CRC, offering opportunities for optimizing these patients' treatment outcomes through tailored therapeutic strategies.

Indexed as

colorectal cancerleft‐sidedphosphoproteomeproteomeright‐sidedwhole‐exome sequencing

Identifiers

PMID42266181
PMCPMC13243882

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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.