Evidence map›Paper›PMID 35203376›Full record

ArticleCells2022

Characterization of Collapsin Response Mediator Protein 2 in Colorectal Cancer Progression in Subjects with Diabetic Comorbidity.

Yih-Hsin Chang, Hui-Ju Yang, Huan-Wen Chen, Chiao-Wan Hsiao, Yi-Chen Hsieh, Yu-Wei Chan, Shu-Wen Chang, Wei-Lun Hwang, Wei-Shone Chen, Hou-Hsuan Cheng and 8 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2022. 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
0.4field-weighted citation impact, top 49% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. The intersection of colorectal cancer and cardiovascular disease: shared mechanisms and clinical implications.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
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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

18 authors at 6 institutions in 1 country.

Yih-Hsin ChangDepartment of Biotechnology and Laboratory Science in Medicine, National Yang Ming Chiao Tung University, Taipei 112, Taiwan.
Hui-Ju YangDepartment of Biotechnology and Laboratory Science in Medicine, National Yang Ming Chiao Tung University, Taipei 112, Taiwan.
Huan-Wen ChenDepartment of Biotechnology and Laboratory Science in Medicine, National Yang Ming Chiao Tung University, Taipei 112, Taiwan.
Chiao-Wan HsiaoDepartment of Biotechnology and Laboratory Science in Medicine, National Yang Ming Chiao Tung University, Taipei 112, Taiwan.
Yi-Chen HsiehDepartment of Biotechnology and Laboratory Science in Medicine, National Yang Ming Chiao Tung University, Taipei 112, Taiwan.
Yu-Wei ChanDepartment of Biotechnology and Laboratory Science in Medicine, National Yang Ming Chiao Tung University, Taipei 112, Taiwan.
Shu-Wen ChangDepartment of Biotechnology and Laboratory Science in Medicine, National Yang Ming Chiao Tung University, Taipei 112, Taiwan.
Wei-Lun HwangDepartment of Biotechnology and Laboratory Science in Medicine, National Yang Ming Chiao Tung University, Taipei 112, Taiwan.ORCID 0000-0002-8694-877X
Wei-Shone ChenDepartment of Medicine, National Yang Ming Chiao Tung University, Taipei 112, Taiwan.
Hou-Hsuan ChengDepartment of Medicine, National Yang Ming Chiao Tung University, Taipei 112, Taiwan.
Teh-Ying ChouDepartment of Pathology and Laboratory Medicine, Taipei Veterans General Hospital, Taipei 112, Taiwan.ORCID 0000-0001-5844-477X
Fu-Pang ChangDepartment of Pathology and Laboratory Medicine, Taipei Veterans General Hospital, Taipei 112, Taiwan.
Hsiang-Ling HoDepartment of Pathology and Laboratory Medicine, Taipei Veterans General Hospital, Taipei 112, Taiwan.
Fang-Yeh ChuDepartment of Clinical Pathology, Far Eastern Memorial Hospital, New Taipei City 220, Taiwan.
Yu-Li LoDepartment and Institute of Pharmacology, National Yang Ming Chiao Tung University, Taipei 112, Taiwan.
Chun-Jung ChenDepartment of Medical Research, Taichung Veterans General Hospital, Taichung 407, Taiwan.
Hui-Fang TsaiDepartment of Medical Laboratory and Biotechnology, Chung Shan Medical University, Taichung 402, Taiwan.
Ming-Yuh ShiauDepartment of Nursing, College of Nursing, Hungkuang University, Taichung 433, Taiwan.
National Yang Ming Chiao Tung University · TWTaipei Veterans General Hospital · TWChina Medical University · TWChung Shan Medical University Hospital · TWHungkuang University · TWYuanpei University · TW

Funding

Ministry of Science and Technology Taiwan MOST 102-2320-B-241-004-MY3, 105-2320-B-241-005 and 110-2314-B-241-001National Yang-Ming University Far Eastern Memorial Hospital Joint Research Program 109DN14 and 110DN17Veterans General Hospitals and University System of Taiwan Joint Research Program VGHUST106-G7-7-1, 108-G2-1-1, 109-V7-3 and 110-G2-2-3
6 · The paper itself

Abstract

backgroundCommon demographic risk factors are identified in colorectal cancer (CRC) and type 2 diabetes mellitus (DM), nevertheless, the molecular link and mechanism for CRC-DM comorbidity remain elusive. Dysregulated glycogen synthase kinase-3 beta under metabolic imbalance is suggested to accelerate CRC pathogenesis/progression via regulating collpasin response mediator protein-2 (CRMP2). Accordingly, roles of CRMP2 in CRC and CRC-DM patients were investigated for elucidating the molecular convergence of CRC and DM.

methodsCRMP2 profile in tumor tissues from CRC and CRC-DM patients was investigated to explore the link between CRC and DM etiology. Meanwhile, molecular mechanism of glucose to regulate CRMP2 profile and CRC characteristics was examined in vitro and in vivo.

resultsCRMP2 was significantly lower in tumor lesions and associated with advanced tumor stage in CRC-DM patients. Physiological hyperglycemia suppressed CRMP2 expression/activity and augmented malignant characteristics of CRC cells. Hyperglycemia promotes actin de-polymerization, cytoskeleton flexibility and cell proliferation/metastasis by downregulating CRMP2 profile and thus contributes to CRC disease progression.

conclusionsThis study uncovers molecular evidence to substantiate and elucidate the link between CRC and T2DM, as well as characterizing the roles of CRMP2 in CRC-DM. Accordingly, altered metabolic adaptations are promising targets for anti-diabetic and cancer strategies.

Indexed as

Colorectal NeoplasmsDiabetes Mellitus, Type 2HyperglycemiaIntercellular Signaling Peptides and ProteinsNerve Tissue ProteinsComorbidityHumansPhosphorylationcollapsin response mediator protein-2Intercellular Signaling Peptides and ProteinsNerve Tissue Proteinscolorectal cancerCRMP2hyperglycemiatype 2 diabetes mellitus

Identifiers

PMID35203376
PMCPMC8869905
OpenAlexW4212963101

What OpenQuestion 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 OpenQuestion graph.