Evidence map›Paper›PMID 39014007›Full record

ArticleNPJ precision oncology2024

WWP1 inhibition increases SHP2 inhibitor efficacy in colorectal cancer.

Hao Fan, Xuefei Hu, Fuao Cao, Leqi Zhou, Rongbo Wen, Hao Shen, Yating Fu, Xiaoming Zhu, Hang Jia, Zixuan Liu and 4 more

Abstract read
In one paragraph

Article in NPJ precision oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Article
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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

14 authors.

Hao Fan *Department of Colorectal Surgery, Changhai Hospital, Naval Medical University, Shanghai, China.ORCID http://orcid.org/0000-0002-3558-0397
Xuefei Hu *Department of Navy Environmental and Occupational Health, Faculty of Naval Medicine, Naval Medical University, Shanghai, China.
Fuao Cao *Department of Colorectal Surgery, Changhai Hospital, Naval Medical University, Shanghai, China.
Leqi Zhou *Department of Colorectal Surgery, Changhai Hospital, Naval Medical University, Shanghai, China.
Rongbo WenDepartment of Colorectal Surgery, Changhai Hospital, Naval Medical University, Shanghai, China.
Hao ShenDepartment of Navy Environmental and Occupational Health, Faculty of Naval Medicine, Naval Medical University, Shanghai, China.
Yating FuDepartment of Navy Environmental and Occupational Health, Faculty of Naval Medicine, Naval Medical University, Shanghai, China.
Xiaoming ZhuDepartment of Colorectal Surgery, Changhai Hospital, Naval Medical University, Shanghai, China.
Hang JiaDepartment of Colorectal Surgery, Changhai Hospital, Naval Medical University, Shanghai, China.
Zixuan LiuDepartment of Colorectal Surgery, Changhai Hospital, Naval Medical University, Shanghai, China.
Guimin WangDepartment of Colorectal Surgery, Changhai Hospital, Naval Medical University, Shanghai, China.
Guanyu YuDepartment of Colorectal Surgery, Changhai Hospital, Naval Medical University, Shanghai, China. yuguanyu0451@163.com.ORCID http://orcid.org/0000-0001-5416-3559
Wenjun ChangDepartment of Navy Environmental and Occupational Health, Faculty of Naval Medicine, Naval Medical University, Shanghai, China. cwjcwj1976@smmu.edu.cn.ORCID http://orcid.org/0000-0002-8476-4731
Wei ZhangDepartment of Colorectal Surgery, Changhai Hospital, Naval Medical University, Shanghai, China. weizhang2000cn@163.com.

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82072750National Natural Science Foundation of China (National Science Foundation of China) 82272705
6 · The paper itself

Abstract

Protein tyrosine phosphatase SHP2 activates RAS signaling, which is a novel target for colorectal cancer (CRC) therapy. However, SHP2 inhibitor monotherapy is ineffective for metastatic CRC and a combination therapy is required. In this study, we aimed to improve the antitumor efficacy of SHP2 inhibition and try to explore the resistance mechanism of SHP2 inhibitor. Results showed that WWP1 promoted the proliferation of CRC cells. Genetic or pharmacological inhibition of WWP1 enhanced the effect of SHP2 inhibitor in suppressing tumor growth in vitro and in vivo. WWP1 may mediate feedback reactivation of AKT signaling following SHP2 inhibition. Furthermore, nomogram models constructed with IHC expression of WWP1 and SHP2 greatly improved the accuracy of prognosis prediction for patients with CRC. Our findings indicate that WWP1 inhibitor I3C can synergize with SHP2 inhibitor and is expected to be a new strategy for clinical trials in treating advanced CRC patients.

Identifiers

PMID39014007
PMCPMC11252267

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.