Association Between CD147 Expression, RAS Mutational Status, and Local Recurrence in Resected Locally Advanced Rectal Cancer.

doi:10.1002/cam4.71087

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Community

Back to search

Article

Association Between CD147 Expression, RAS Mutational Status, and Local Recurrence in Resected Locally Advanced Rectal Cancer.

Cancer medicine - 1 Aug 2025

Isnard Anaëlle, Cramier Laure-Amandine, Vergara Rémi, Boubaddi Mehdi, Fouche Donatien, Fernandez Benjamin, Senant Nathalie, Denost Quentin, Rullier Éric, Dubus Pierre, Dabernat Sandrine, Dupin Charles, Vendrely Véronique, Rullier Anne, Amintas Samuel

Abstract excerpt

AIM: About 5% to 10% of rectal cancer (RC) patients experience local disease recurrence after chemoradiotherapy (CRT) and surgery. Identifying patients at high risk of local recurrence (LR) could lead to the personalized management of the patients. Multiple clinicopathological parameters are associated with LR. However, the potential of tumors for local regrowth may partially lie in the expression of pro-tumoral...

Read the complete abstract on PubMed

Topics

Humans
Male
Female
Rectal Neoplasms
Basigin

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Neoplasm Recurrence, Local

Middle Aged

Aged

Retrospective Studies

Mutation

Biomarkers, Tumor

Adult

Source

Open in PubMed Open full text

Identifiers

PMID: 40727998
DOI: 10.1002/cam4.71087
PMCID: PMC12305349

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 24 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Association Between CD147 Expression, RAS Mutational Status, and Local Recurrence in Resected Locally Advanced Rectal Cancer.PMID 40727998Read ↗

KRAS Mutant Status May Be Associated with Distant Recurrence in Early-stage Rectal Cancer.Semantic proximity Read ↗

Clinical and genetic factors associated with tumor response to neoadjuvant (chemo)radiotherapy, survival and recurrence risk in rectal cancer.Semantic proximity Read ↗

Molecular predictors of treatment resistance and recurrence following neoadjuvant therapy in rectal cancer.Semantic proximity Read ↗

Impact of RAS/BRAF mutation status in locally advanced rectal cancer treated with preoperative chemotherapy.Semantic proximity Read ↗

KRAS Mutant Status, p16 and β-catenin Expression May Predict Local Recurrence in Patients Who Underwent Transanal Endoscopic Microsurgery (TEMS) for Stage I Rectal Cancer.Semantic proximity Read ↗

Identification of a biomarker profile associated with resistance to neoadjuvant chemoradiation therapy in rectal cancer.Semantic proximity Read ↗

Tumor microRNAs Identified by Small RNA Sequencing as Potential Response Predictors in Locally Advanced Rectal Cancer Patients Treated With Neoadjuvant ChemoradiotherapySemantic proximity Read ↗

Prognostic Impact of Ras Mutation on Surgical Strategy in Rectal Cancer Patients Undergoing Neoadjuvant Treatment.Semantic proximity Read ↗

Molecular differentiation between complete and incomplete responders to neoadjuvant therapy in rectal cancerSemantic proximity Read ↗

Negative prognostic impact of Co-mutations in TGFβ and TP53 pathways in surgically resected rectal tumors following neoadjuvant chemoradiotherapy.Semantic proximity Read ↗

Epithelial mesenchymal transition and resistance to neoadjuvant radiotherapy in locally advanced rectal cancerSemantic proximity Read ↗

Predictive role of microRNA-related genetic polymorphisms in the pathological complete response to neoadjuvant chemoradiotherapy in locally advanced rectal cancer patients.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.