Evidence map›Paper›PMID 42621110›Full record

ArticleiScience2026

CPS1 promotes colorectal cancer progression by inducing EMT and activating TGF-β/Smad signaling pathway.

Ning Qu, Jinglian Chen, Yanlu Chen, Sicheng Zhao, Yuman Wu, Jincan Wei, Shang Lou, Yanrong Liao, Yonghai Yan, Tao Luo and 2 more

Abstract read
In one paragraph

Article in iScience, 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.

Ning QuColorectal and Anal Disease Unit, Department of Gastrointestinal Surgery, Guangxi Medical University Cancer Hospital, Nanning, Guangxi, China.
Jinglian ChenColorectal and Anal Disease Unit, Department of Gastrointestinal Surgery, Guangxi Medical University Cancer Hospital, Nanning, Guangxi, China.
Yanlu ChenColorectal and Anal Disease Unit, Department of Gastrointestinal Surgery, Guangxi Medical University Cancer Hospital, Nanning, Guangxi, China.
Sicheng ZhaoColorectal and Anal Disease Unit, Department of Gastrointestinal Surgery, Guangxi Medical University Cancer Hospital, Nanning, Guangxi, China.
Yuman WuColorectal and Anal Disease Unit, Department of Gastrointestinal Surgery, Guangxi Medical University Cancer Hospital, Nanning, Guangxi, China.
Jincan WeiColorectal and Anal Disease Unit, Department of Gastrointestinal Surgery, Guangxi Medical University Cancer Hospital, Nanning, Guangxi, China.
Shang LouColorectal and Anal Disease Unit, Department of Gastrointestinal Surgery, Guangxi Medical University Cancer Hospital, Nanning, Guangxi, China.
Yanrong LiaoColorectal and Anal Disease Unit, Department of Gastrointestinal Surgery, Guangxi Medical University Cancer Hospital, Nanning, Guangxi, China.
Yonghai YanColorectal and Anal Disease Unit, Department of Gastrointestinal Surgery, Guangxi Medical University Cancer Hospital, Nanning, Guangxi, China.
Tao LuoColorectal and Anal Disease Unit, Department of Gastrointestinal Surgery, Guangxi Medical University Cancer Hospital, Nanning, Guangxi, China.
Wenqi LuoGuangxi Key Laboratory of Basic and Translational Research for Colorectal Cancer, Guangxi Medical University Cancer Hospital, Nanning, Guangxi, China.
Qi ZengGuangxi Key Laboratory of Basic and Translational Research for Colorectal Cancer, Guangxi Medical University Cancer Hospital, Nanning, Guangxi, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer (CRC) is a highly lethal digestive malignancy, particularly in metastatic cases. Carbamoyl-phosphate synthase 1 (CPS1), a key mitochondrial enzyme involved in the urea cycle, has been implicated in multiple cancers. However, its role in CRC remains poorly understood. This study demonstrated that CPS1 expression was significantly upregulated in CRC tissues and was associated with aggressive clinicopathological characteristics and poor prognosis. Functional experiments revealed that CPS1 knockdown markedly suppressed CRC cell proliferation, migration, invasion, and tumorigenicity, whereas CPS1 overexpression exerted opposite effects. Mechanistically, CPS1 downregulation increased E-cadherin expression and decreased the expression of ZEB1, slug, N-cadherin, vimentin, MMP2, and

Indexed as

carbamoyl-phosphate synthase 1colorectal cancerepithelial-mesenchymal transitionmetastasisTGF-β signal

Identifiers

PMID42621110
PMCPMC13486773

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.