Clinical significance of epithelial-mesenchymal transition-related markers expression in the micrometastatic sentinel lymph node of NSCLC.


Journal

Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico
ISSN: 1699-3055
Titre abrégé: Clin Transl Oncol
Pays: Italy
ID NLM: 101247119

Informations de publication

Date de publication:
Mar 2020
Historique:
received: 11 01 2019
accepted: 21 05 2019
pubmed: 28 5 2019
medline: 18 11 2020
entrez: 29 5 2019
Statut: ppublish

Résumé

Metastatic lymph node affectation is the main prognostic factor in localised lung cancer. However, the pathological study of lymph nodes reveals tumour relapse for 20% of patients after oncological curative surgery. Recently, EMT (epithelial-mesenchymal transition) has been established as one of the main factors related to lymphatic dissemination and metastasis. This study evaluated the prognostic value of EMT-related gene expression in micrometastatic sentinel lymph nodes (SLN) of non-small cell lung cancer (NSCLC) patients. The presence of genes CDH1, CDH2, VIM, TWIST1, SNAI1, SNAI2, ZEB1, and ZEB2 in mRNA was analysed in tumours and in the SLN of NSCLC patients for whom surgery was planned for treatment. The significant association between the expression level of EMT-related markers and patients' clinicopathological characteristics and relapse was assessed. Of the 96 patients, 56 (58.33%) presented molecular micrometastasis in SLN, which showed higher CDH1, CDH2, and VIM expressions than non-micrometastatic ones. An association linking a low CDH1/CDH2 ratio in SLN with molecular micrometastasis, adenocarcinoma, and non-smoking patients was found. The multivariate Cox regression analysis proved the prognostic accuracy of the CDH1/CDH2 ratio in SLN. The molecular EMT status of SLN could be used as an independent prognosis predictor in early stage NSLCL patients, and as a new tool to better stratify and predict patient outcomes.

Identifiants

pubmed: 31134511
doi: 10.1007/s12094-019-02138-3
pii: 10.1007/s12094-019-02138-3
doi:

Substances chimiques

Antigens, CD 0
Biomarkers, Tumor 0
CDH1 protein, human 0
CDH2 protein, human 0
Cadherins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

381-391

Subventions

Organisme : FISABIO
ID : UGP-15-137

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Auteurs

A Lafuente-Sanchis (A)

Department of Molecular Biology, Hospital Universitario de la Ribera, Ctra. Corbera, km. 1, 46600, Alzira, Spain. lafuentesanchisaranzazu@gmail.com.

A Olmo (A)

Department of Thoracic Surgery, Hospital Universitario de la Ribera, Alcira, Spain.

J Carretero (J)

Department of Physiology, Facultad de Farmacia, Universidad de Valencia, Valencia, Spain.

J Alcacer Fernandez-Coronado (J)

Department of Pathology, Hospital Quirón Valencia, Valencia, Spain.

M Estors-Guerrero (M)

Department of Thoracic Surgery, Hospital Universitario de la Ribera, Alcira, Spain.

N J Martínez-Hernández (NJ)

Department of Thoracic Surgery, Hospital Universitario de la Ribera, Alcira, Spain.

A Cremades (A)

Department of Pathology, Hospital Universitario de la Ribera, Alcira, Spain.

A Zúñiga (A)

Department of Molecular Biology, Hospital Universitario de la Ribera, Ctra. Corbera, km. 1, 46600, Alzira, Spain.

J Alcacer (J)

Department of Pathology, Hospital Quirón Valencia, Valencia, Spain.

R Farras (R)

Laboratory of Oncogenic Signaling, Centro de Investigación Príncipe Felipe, Valencia, Spain.

M Cuenca (M)

Department of Molecular Biology, Hospital Universitario de la Ribera, Ctra. Corbera, km. 1, 46600, Alzira, Spain.

J M Galbis-Caravajal (JM)

Department of Thoracic Surgery, Hospital Universitario de la Ribera, Alcira, Spain.

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Classifications MeSH