Evidence map›Paper›PMID 42226795›Full record

ArticleCancer informatics2026

iCRCexp: An Integrative Database for Colorectal Cancer-Associated Gene Expression Profiles.

Yan Yuan, Bi-Jin Cao, Zhi-Kai Qian, Ze-Kun Liu, Wei-Wei Xiao, Xing-Yang Li, Zhi-Xiang Zuo, Ze-Xian Liu, Yuan-Hong Gao

Abstract read
In one paragraph

Article in Cancer informatics, 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

9 authors.

Yan YuanDepartment of Medical Oncology, Affiliated Cancer Hospital and Institute of Guangzhou Medical University, PR China.
Bi-Jin CaoSchool of Life Sciences, Zhengzhou University, PR China.
Zhi-Kai QianGuangdong Provincial Clinical Research Center for Cancer, Guangzhou, PR China.
Ze-Kun LiuGuangdong Provincial Clinical Research Center for Cancer, Guangzhou, PR China.
Wei-Wei XiaoGuangdong Provincial Clinical Research Center for Cancer, Guangzhou, PR China.
Xing-Yang LiKey Laboratory of Oral Medicine, Guangzhou Institute of Oral Disease, Affiliated Stomatology Hospital of Guangzhou Medical University, China.
Zhi-Xiang ZuoGuangdong Provincial Clinical Research Center for Cancer, Guangzhou, PR China.
Ze-Xian LiuGuangdong Provincial Clinical Research Center for Cancer, Guangzhou, PR China.
Yuan-Hong GaoGuangdong Provincial Clinical Research Center for Cancer, Guangzhou, PR China.ORCID https://orcid.org/0000-0002-6429-5376

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Colorectal cancer (CRC) is a leading cause of tumor-related mortality. Recent studies have shown that the transcriptome plays an important role in the development and occurrence of CRC. However, a comprehensive repository of CRC transcriptome sequencing data is unavailable. In the present study, we constructed a colorectal database (iCRCexp; http://icrcexp.omicsbio.info/). Method: We collected CRC-related transcriptome datasets from The Cancer Genome Atlas (TCGA) and National Center for Biotechnology Information (NCBI) Gene Ontology Omnibus (GEO) databases up to 2022. The sequencing data were preprocessed through a unified pipeline and subsequently analyzed. CRC-related genes and drugs were identified via text mining of the PubMed abstracts. Results: A total of 18 466 tissue samples from 231 studies, 2429 CRC-related genes, and 1852 CRC-related drugs were collected and integrated into iCRCexp. Among these studies, 251 CRC-related datasets were identified with abundant characteristic information, including tissue source, baseline characteristics, therapeutic responses, recurrence and metastasis, and survival. We conducted differential correlation and survival analyses. We predicted potential target drugs for CRC-related genes by calculating connectivity scores. Consequently, we integrated these analysis results through network construction and presented them in a CRC database. Conclusion: A comprehensive resource, including CRC-related gene and medication information and an expression analysis platform, was constructed for the CRC community.

Indexed as

colorectal cancerdatabasedrug predictioniCRCexptranscriptome

Identifiers

PMID42226795
PMCPMC13222402

What Socratic holds

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Registered trials

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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 Socratic graph.