Evidence map›Paper›PMID 35273688›Full record

ArticleAmerican journal of translational research2022

TRIM24 promotes colorectal cancer cell progression via the Wnt/β-catenin signaling pathway activation.

Hong Tian, Hongmei Zhao, Bo Qu, Xiaoli Chu, Xing Xin, Qingwei Zhang, Weizhou Li, Shida Yang

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 21% of its field
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

15 citing papers in PubMed, 9 citations in OpenAlex.

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  11. Nutrients · 2024
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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

8 authors at 1 institution in 1 country.

Hong TianOncology Department, The 4th People's Hospital of Shenyang Shenyang 110013, Liaoning, China.
Hongmei ZhaoDepartment of Laboratory Medicine, The People's Hospital of China Medical University (The People's Hospital of Liaoning Province) Shenyang 110016, Liaoning, China.
Bo QuDepartment of Laboratory Medicine, The People's Hospital of China Medical University (The People's Hospital of Liaoning Province) Shenyang 110016, Liaoning, China.
Xiaoli ChuOncology Department, The 4th People's Hospital of Shenyang Shenyang 110013, Liaoning, China.
Xing XinOncology Department, The 4th People's Hospital of Shenyang Shenyang 110013, Liaoning, China.
Qingwei ZhangGeneral Surgery Dept. VI Ward (Biliary-Pancreatic Surgery), The People's Hospital of China Medical University (The People's Hospital of Liaoning Province) Shenyang 110016, Liaoning, China.
Weizhou LiDepartment of Laboratory Medicine, The People's Hospital of China Medical University (The People's Hospital of Liaoning Province) Shenyang 110016, Liaoning, China.
Shida YangDepartment of Laboratory Medicine, The People's Hospital of China Medical University (The People's Hospital of Liaoning Province) Shenyang 110016, Liaoning, China.
Liaoning Provincial People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Overexpression of TRIM24 is observed in several human cancers and is correlated with an increase in the progression and metastasis of tumors. In this study, we investigated the changes in activity and biochemical events that occur after overexpression of TRIM24 in a colorectal cancer (CRC) mouse model. We observed upregulated TRIM24 expression in CRC tissues compared to that in nonneoplastic adjacent tissues. Enhanced expression of TRIM24 was significantly associated with the status of lymph nodes and poor recurrence-free survival of patients with CRC. The role of TRIM24 in CRC tumor growth was investigated using an orthotopic model of MC38 mouse colon cancer cells overexpressing TRIM24, and CRC tumor growth was found to increase dramatically by TRIM24 overexpression. Moreover, angiogenesis was stimulated by TRIM24 overexpression via the upregulation of vascular endothelial growth factor (VEGF) expression. Overexpression of TRIM24 in MC38 cells led to an increase in the protein levels of ALDH1 and other stem cell markers. In addition, we observed that Wnt/β-catenin signaling is required for the function of TRIM24 in CRC cells. Tumor-associated macrophages (TAMs) were found to be recruited by tumor cells overexpressing TRIM24 via the increased expression of CCL2/5, CSF-1, and VEGF, further enhancing CRC tumor growth. In conclusion, overexpression of TRIM24 facilitates the growth of CRC and the remodeling of the tumor stroma via angiogenesis stimulation and TAM recruitment. The Wnt/β-catenin pathway is a possible crucial link in the TRIM24-associated progression of tumors, which may provide opportunities for pharmacological intervention.

Indexed as

angiogenesisCRCstem-like cellsTAMTRIM24

Identifiers

PMID35273688
PMCPMC8902576
OpenAlexW4226186690

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.