Evidence map›Paper›PMID 40664638›Full record

ArticleCell death & disease2025

Modeling oxaliplatin resistance in colorectal cancer reveals a SERPINE1-based gene signature (RESIST-M) and therapeutic strategies for pro-metastatic CMS4 subtype.

Stephen Qi Rong Wong, Mohua Das, Kenzom Tenzin, Niranjan Shirgaonkar, Huiwen Chua, Lin Xuan Chee, Ahpa Sae Yeoh, Astley Aruna Murugiah, Wei Yong Chua, Madelaine Skolastika Theardy and 9 more

Abstract read
In one paragraph

Article in Cell death & disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

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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

19 authors.

Stephen Qi Rong Wong *Genome Institute of Singapore, Laboratory of Precision Oncology and Cancer Evolution, Agency for Science, Technology and Research, Singapore, Singapore.ORCID http://orcid.org/0000-0002-8906-6465
Mohua Das *Genome Institute of Singapore, Laboratory of Precision Oncology and Cancer Evolution, Agency for Science, Technology and Research, Singapore, Singapore.
Kenzom Tenzin *Genome Institute of Singapore, Laboratory of Precision Oncology and Cancer Evolution, Agency for Science, Technology and Research, Singapore, Singapore.
Niranjan ShirgaonkarGenome Institute of Singapore, Laboratory of Precision Oncology and Cancer Evolution, Agency for Science, Technology and Research, Singapore, Singapore.ORCID http://orcid.org/0000-0001-6078-1409
Huiwen ChuaGenome Institute of Singapore, Laboratory of Precision Oncology and Cancer Evolution, Agency for Science, Technology and Research, Singapore, Singapore.
Lin Xuan CheeGenome Institute of Singapore, Laboratory of Precision Oncology and Cancer Evolution, Agency for Science, Technology and Research, Singapore, Singapore.
Ahpa Sae YeohGenome Institute of Singapore, Laboratory of Precision Oncology and Cancer Evolution, Agency for Science, Technology and Research, Singapore, Singapore.
Astley Aruna MurugiahGenome Institute of Singapore, Laboratory of Precision Oncology and Cancer Evolution, Agency for Science, Technology and Research, Singapore, Singapore.
Wei Yong ChuaGenome Institute of Singapore, Laboratory of Precision Oncology and Cancer Evolution, Agency for Science, Technology and Research, Singapore, Singapore.ORCID http://orcid.org/0009-0004-8461-9552
Madelaine Skolastika TheardyGenome Institute of Singapore, Laboratory of Precision Oncology and Cancer Evolution, Agency for Science, Technology and Research, Singapore, Singapore.
Ethan Jadon SubelDepartment of Urology, Methodist Neal Cancer Center, Houston Methodist Research Institute, Houston, TX, USA.
Matan Thangavelu ThangaveluEDDC Academic Research Organization, Agency for Science, Technology and Research, Singapore, Singapore.
Jane Vin ChanGenome Institute of Singapore, Laboratory of Precision Oncology and Cancer Evolution, Agency for Science, Technology and Research, Singapore, Singapore.
Choon Kong YapNational Cancer Center Singapore, Laboratory of Translational Research in Gastrointestinal Cancer, Singapore, Singapore.
Iain Bee Huat TanNational Cancer Center Singapore, Laboratory of Translational Research in Gastrointestinal Cancer, Singapore, Singapore.
Petros TsantoulisCentre for Translational Research in Onco-Hematology, Faculty of Medicine, University of Geneva, and Swiss Cancer Centre Leman, Geneva, Switzerland.ORCID http://orcid.org/0000-0003-3613-6682
Sabine TejparMolecular Digestive Oncology, Department of Oncology, Katholieke Universiteit Leuven, Leuven, Belgium.ORCID http://orcid.org/0000-0003-3281-8643
Jia Min LooGenome Institute of Singapore, Laboratory of Precision Oncology and Cancer Evolution, Agency for Science, Technology and Research, Singapore, Singapore.
Ramanuj DasGuptaGenome Institute of Singapore, Laboratory of Precision Oncology and Cancer Evolution, Agency for Science, Technology and Research, Singapore, Singapore. ramanuj.dasgupta@glasgow.ac.uk.ORCID http://orcid.org/0000-0001-9015-3729

Funding

Genome Institute of Singapore (GIS) Core fundsMOH | National Medical Research Council (NMRC) NMRC/CIRG/1439/2015MOH | National Medical Research Council (NMRC) NMRC/OFIRG/0025/2019National Research Foundation Singapore (National Research Foundation-Prime Minister's office, Republic of Singapore) NRF-CRP26-2021-0005
6 · The paper itself

Abstract

Drug resistance and distant metastases are leading causes of mortality in colorectal cancer (CRC), yet the molecular mechanisms linking these processes remain elusive. In this study, we demonstrate that acquired resistance to oxaliplatin, a first-line chemotherapeutic in CRC, enhances metastatic potential through transcriptional reprogramming. Using a clinically relevant dosing regimen, we generated oxaliplatin-resistant CRC cells that displayed increased metastatic potential. Integrated transcriptomic and phenotypic analyses revealed that dysregulated cholesterol biogenesis amplifies TGF-β signaling, which in turn drives expression of SERPINE1, which serves as a key effector of both oxaliplatin resistance and metastasis. Furthermore, we uncovered a SERPINE1-associated nine-gene expression signature, RESIST-M, that robustly predicts overall and relapse-free survival across distinct patient cohorts. Notably, RESIST-M stratifies a high-risk subtype of CMS4/iCMS3-fibrotic patients that display the poorest prognosis, underscoring its clinical relevance. Targeting of SERPINE1 or cholesterol biosynthesis re-sensitized resistant, pro-metastatic cells to oxaliplatin in mouse xenograft models. Altogether, this study uncovers a mechanistic link between metabolic rewiring and transcriptional plasticity underlying therapy-induced metastasis in primary CRC. Additionally, it also reveals actionable vulnerabilities that offer both prognostic value and therapeutic potential.

Indexed as

Colorectal NeoplasmsDrug Resistance, NeoplasmOxaliplatinPlasminogen Activator Inhibitor 1AnimalsAntineoplastic AgentsCell Line, TumorCholesterolGene Expression Regulation, NeoplasticHumansMiceNeoplasm MetastasisSignal TransductionXenograft Model Antitumor AssaysAntineoplastic AgentsCholesterolOxaliplatinPlasminogen Activator Inhibitor 1SERPINE1 protein, human

Identifiers

PMID40664638
PMCPMC12264272

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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.