Evidence map›Paper›PMID 40185866›Full record

ArticleCommunications biology2025

TCP1 promotes the progression of malignant tumours by stabilizing c-Myc through the AKT/GSK-3β and ERK signalling pathways.

Hekun Liu, Linying Chen, Yuwen Chen, Yiyi Jin, Xiance Chen, Nengjun Ma, Fan Yang, Huixia Bi, Xinxin Wen, Shenmin Xu and 5 more

Abstract read
In one paragraph

Article in Communications biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Translational cancer research · 2025
    Article
  4. Review
  5. Article
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

15 authors.

Hekun Liu *Fujian Key Laboratory of Translational Research in Cancer and Neurodegenerative Diseases, The School of Basic Medical Sciences, Fujian Medical University, No. 1, Xuefu North Road, 350122, Fuzhou, Fujian, China.
Linying Chen *Department of Pathology, the First Affiliated Hospital of Fujian Medical University, No. 20, Chazhong Road, 350005, Fuzhou, Fujian, China.
Yuwen ChenFujian Key Laboratory of Translational Research in Cancer and Neurodegenerative Diseases, The School of Basic Medical Sciences, Fujian Medical University, No. 1, Xuefu North Road, 350122, Fuzhou, Fujian, China.
Yiyi JinFujian Key Laboratory of Translational Research in Cancer and Neurodegenerative Diseases, The School of Basic Medical Sciences, Fujian Medical University, No. 1, Xuefu North Road, 350122, Fuzhou, Fujian, China.
Xiance ChenFujian Key Laboratory of Translational Research in Cancer and Neurodegenerative Diseases, The School of Basic Medical Sciences, Fujian Medical University, No. 1, Xuefu North Road, 350122, Fuzhou, Fujian, China.
Nengjun MaFujian Key Laboratory of Translational Research in Cancer and Neurodegenerative Diseases, The School of Basic Medical Sciences, Fujian Medical University, No. 1, Xuefu North Road, 350122, Fuzhou, Fujian, China.
Fan YangFujian Key Laboratory of Translational Research in Cancer and Neurodegenerative Diseases, The School of Basic Medical Sciences, Fujian Medical University, No. 1, Xuefu North Road, 350122, Fuzhou, Fujian, China.
Huixia BiFujian Key Laboratory of Translational Research in Cancer and Neurodegenerative Diseases, The School of Basic Medical Sciences, Fujian Medical University, No. 1, Xuefu North Road, 350122, Fuzhou, Fujian, China.
Xinxin WenFujian Key Laboratory of Translational Research in Cancer and Neurodegenerative Diseases, The School of Basic Medical Sciences, Fujian Medical University, No. 1, Xuefu North Road, 350122, Fuzhou, Fujian, China.
Shenmin XuFujian Key Laboratory of Translational Research in Cancer and Neurodegenerative Diseases, The School of Basic Medical Sciences, Fujian Medical University, No. 1, Xuefu North Road, 350122, Fuzhou, Fujian, China.
Juan ChenFujian Key Laboratory of Translational Research in Cancer and Neurodegenerative Diseases, The School of Basic Medical Sciences, Fujian Medical University, No. 1, Xuefu North Road, 350122, Fuzhou, Fujian, China.
Yanping LinFujian Key Laboratory of Translational Research in Cancer and Neurodegenerative Diseases, The School of Basic Medical Sciences, Fujian Medical University, No. 1, Xuefu North Road, 350122, Fuzhou, Fujian, China.
Yinghong YangDepartment of Pathology, Fujian Medical University Union Hospital, No. 29, Xinquan Road, Fuzhou, Fujian, 350001, China.
Yong WuFujian Institute of Haematology, Fujian Key Laboratory on Haematology, Fujian Medical University Union Hospital, No. 29, Xinquan Road, 350001, Fuzhou, Fujian, China. wuyong9195@126.com.ORCID http://orcid.org/0000-0002-2873-0334
Yuanzhong ChenFujian Institute of Haematology, Fujian Key Laboratory on Haematology, Fujian Medical University Union Hospital, No. 29, Xinquan Road, 350001, Fuzhou, Fujian, China. chenyz@fjmu.edu.cn.ORCID http://orcid.org/0000-0002-9411-1427

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The chaperonin tailless complex polypeptide 1 (TCP1) is a key subunit of chaperonin containing TCP1 (CCT) that regulates the folding and stability of proteins during cancer progression. Here, the prognostic significance of TCP1 was explored mainly in patients with hepatocellular carcinoma (HCC) and pancreatic ductal adenocarcinoma (PDAC). We showed that TCP1 expression was significantly greater in clinically malignant tumour tissues than in normal tissues and that high TCP1 expression was associated with poor prognosis. TCP1 suppression not only decreased the proliferation and invasion of cancer cells in vitro but also inhibited tumour growth and metastasis in vivo. The underlying mechanisms were determined by ubiquitination assays and Co-IP (Co-Immunoprecipitation) experiments, and it was found that TCP1 regulated the stability of c-Myc through the RAC-alpha serine/threonine-protein kinase (AKT) /Glycogen synthase kinase 3β (GSK-3β) and extracellular regulated protein kinases (ERK) signalling pathways. Moreover, TCP1 knock-in (TCP1-KI) dramatically promoted the occurrence of diethylnitrosamine (DEN) -induced primary HCC in mice. Our results highlight the critical role of TCP1 in HCC and PDAC and reveal a novel mechanism to suppress HCC and PDAC by targeting c-Myc via the TCP1-induced promotion of the AKT/GSK-3β and ERK signalling pathways. TCP1 is able to modulate the stability of target proteins by multiple pathways, thus promoting the progression of HCC and PDAC. Our study identifies TCP1 as a prognostic novel marker and therapeutic target of HCC and PDAC.

Indexed as

Carcinoma, HepatocellularCarcinoma, Pancreatic DuctalChaperonin Containing TCP-1Glycogen Synthase Kinase 3 betaLiver NeoplasmsMAP Kinase Signaling SystemPancreatic NeoplasmsProto-Oncogene Proteins c-aktProto-Oncogene Proteins c-mycAnimalsCell Line, TumorCell ProliferationDisease ProgressionFemaleGene Expression Regulation, NeoplasticHumansChaperonin Containing TCP-1Glycogen Synthase Kinase 3 betaMYC protein, humanProto-Oncogene Proteins c-aktProto-Oncogene Proteins c-myc

Identifiers

PMID40185866
PMCPMC11971430

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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 OpenQuestion graph.