Evidence map›Paper›PMID 39294858›Full record

ArticleJournal of cellular and molecular medicine2024

Single-cell RNA sequencing reveals the heterogeneity of MYH11+ tumour-associated fibroblasts between left-sided and right-sided colorectal cancer.

Chao Wang, Yue Zhao, Sainan Zhang, Meiyu Du, Guanzhi He, Senwei Tan, Hailong Li, Duoyi Zhang, Liang Cheng

Abstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Review
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  12. Oncology research · 2025
    Article
  13. Article
  14. Cell cycle (Georgetown, Tex.)
    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

9 authors.

Chao WangCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, China.
Yue ZhaoCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, China.
Sainan ZhangCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, China.
Meiyu DuCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, China.
Guanzhi HeCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, China.
Senwei TanCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, China.
Hailong LiCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, China.
Duoyi ZhangThe 2nd Affiliated Hospital of Harbin Medical University, Harbin Medical University, Harbin, Heilongjiang, China.
Liang ChengCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, China.ORCID 0000-0002-6665-6710

Funding

National Natural Science Foundation of China 62172130National Natural Science Foundation of China 62222104Tou-Yan Innovation Team Program of the Heilongjiang Province 2019-15
6 · The paper itself

Abstract

Colorectal cancer (CRC) exhibits considerable heterogeneity on tumour location. However, there is still a lack of comprehensive annotation regarding the characteristics and differences between the left-sided (L-CRC) and right-sided (R-CRC) CRC. Here, we performed single-cell RNA sequencing (scRNA-seq) on immune and stromal cells from 12 L-CRC and 10 R-CRC patients. We found that L-CRC exhibited stronger tumour invasion and poor prognosis compared with R-CRC. In addition, functional enrichment analysis of a normal cohort showed that fibroblasts of left colon are associated with tumour-related pathways. This suggested that the heterogeneity observed in both L-CRC and R-CRC may be influenced by the specific location within the colon itself. Further, we identified a potentially novel MYH11+ cancer-associated fibroblast (CAF) subset predominantly enriched in L-CRC. Moreover, we found that MYH11+ CAFs may promote tumour migration via interacting with macrophages, and was associated with poor prognosis in CRC. In summary, our study revealed the crucial role of MYH11+ CAFs in predicting a poor prognosis, thereby contributing valuable insights to the exploration of heterogeneity in L-CRC and R-CRC.

Indexed as

Cancer-Associated FibroblastsColorectal NeoplasmsMyosin Heavy ChainsSingle-Cell AnalysisAgedBiomarkers, TumorCell MovementFemaleGenetic HeterogeneityHumansMaleMiddle AgedPrognosisSequence Analysis, RNABiomarkers, TumorMYH11 protein, humanMyosin Heavy Chainscolorectal cancerleft‐sided and right‐sided colorectal cancersingle cell

Identifiers

PMID39294858
PMCPMC11410558

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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.