Evidence mapPaperPMID 41826571Full record

ReviewMolecular biomedicine2026

Colorectal cancer pathogenesis, oncogenic signaling networks and targeted therapeutic advances.

Yue Chen, Jiaqi Zhang, Yi Ding, Fang Zhu, Yinnan Chen

Abstract readReview
In one paragraph

Review in Molecular biomedicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
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

5 authors.

Yue ChenCenter for Gut Microbiome Research, Med-X Institute, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Jiaqi ZhangCenter for Gut Microbiome Research, Med-X Institute, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Yi DingCenter for Gut Microbiome Research, Med-X Institute, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Fang ZhuHubei Province Key Laboratory of Precision Radiation Oncology, Wuhan, China. zhufang1226@126.com.
Yinnan ChenCenter for Gut Microbiome Research, Med-X Institute, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China. superyaami@163.com.ORCID http://orcid.org/0000-0002-6236-6767

Funding

Natural Science Foundation of Hubei Province No. 2024AFD439Open Research Fund of Hubei Province Key Laboratory of Precision Radiation Oncology 2024ZLJZFL018 2024ZLJZFL026Sand Land-Associated Diseases Research Institute "Open Challenge" Key Research project LN-202410
6 · The paper itself

Abstract

Colorectal cancer (CRC) constitutes a prominent global health burden, being the third most frequently diagnosed malignancy in terms of incidence and the second leading cause of cancer-associated death across the globe. Malignant transformation of colonic epithelial cells stems from the intricate dysregulation of intracellular signal transduction networks. Although targeted therapies have substantially improved patient survival relative to traditional treatments, the complexity of the molecular networks driving carcinogenesis continues to limit the overall prognosis. This review delineates the core signaling cascades governing CRC initiation and progression, with emphasis on the molecular hallmarks of the disease. Drawing on a growing body of high-quality preclinical and clinical evidence, we summarize currently available targeted agents and critically evaluate their underlying mechanisms of action and clinical curative effects, and inherent limitations within the contemporary therapeutic landscape. In addition, we discuss how recent advances in immune checkpoint inhibitors (ICIs) along with a deeper understanding of the tumor microenvironment are shaping global clinical guidelines and revealing promising new targets and combinatorial strategies. In summary, expanding insights into oncogenic signaling pathways are guiding the development of novel treatments and enabling the identification of key elements amenable to pharmacological intervention. Ultimately, this review aims to support the rational design of precise and personalized therapeutic strategies to improve CRC prognosis.

Indexed as

CarcinogenesisColorectal NeoplasmsMolecular Targeted TherapySignal TransductionAnimalsAntineoplastic AgentsHumansTumor MicroenvironmentAntineoplastic AgentsColorectal CancerPathogenesisTargeted inhibitorsTargeted Therapy

Identifiers

PMID41826571
PMCPMC12988139

What Socratic 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 Socratic graph.