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Novel Mouse Cell Lines and In Vivo Models for Human High-Grade Neuroendocrine Lung Carcinoma, Small Cell Lung Carcinoma (SCLC), and Large Cell Neuroendocrine Carcinoma (LCNEC).
Recuero, Enrique; Lázaro, Sara; Lorz, Corina; Enguita, Ana Belén; Garcia-Escudero, Ramón; Santos, Mirentxu.
Afiliación
  • Recuero E; Molecular Oncology Unit, Centro de Investigaciones Energéticas, Medioambientales y Tecnológicas (CIEMAT), 28040 Madrid, Spain.
  • Lázaro S; Molecular Oncology Unit, Centro de Investigaciones Energéticas, Medioambientales y Tecnológicas (CIEMAT), 28040 Madrid, Spain.
  • Lorz C; Molecular Oncology Unit, Centro de Investigaciones Energéticas, Medioambientales y Tecnológicas (CIEMAT), 28040 Madrid, Spain.
  • Enguita AB; Institute of Biomedical Research Hospital "12 de Octubre" (imas12), 28041 Madrid, Spain.
  • Garcia-Escudero R; Tumor Progression Mechanisms Program, CIBERONC, Centro de Investigación Biomédica en Red de Cáncer, 28029 Madrid, Spain.
  • Santos M; Pathology Department, University Hospital "12 de Octubre", 28041 Madrid, Spain.
Int J Mol Sci ; 24(20)2023 Oct 18.
Article en En | MEDLINE | ID: mdl-37894963
ABSTRACT
There is a clear need to expand the toolkit of adequate mouse models and cell lines available for preclinical studies of high-grade neuroendocrine lung carcinoma (small cell lung carcinoma (SCLC) and large cell neuroendocrine carcinoma (LCNEC)). SCLC and LCNEC are two highly aggressive tumor types with dismal prognoses and few therapeutic options. Currently, there is an extreme paucity of material, particularly in the case of LCNEC. Given the lack of murine cell lines and transplant models of LCNEC, the need is imperative. In this study, we generated and examined new models of LCNEC and SCLC transplantable cell lines derived from our previously developed primary mouse LCNEC and SCLC tumors. RNA-seq analysis demonstrated that our cell lines and syngeneic tumors maintained the transcriptome program from the original transgenic primary tumor and displayed strong similarities to human SCLC or LCNEC. Importantly, the SCLC transplanted cell lines showed the ability to metastasize and mimic this characteristic of the human condition. In summary, we generated mouse cell line tools that allow further basic and translational research as well as preclinical testing of new treatment strategies for SCLC and LCNEC. These tools retain important features of their human counterparts and address the lack of LCNEC disease models.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Carcinoma de Células Pequeñas / Carcinoma Neuroendocrino / Carcinoma de Células Grandes / Carcinoma Pulmonar de Células Pequeñas / Neoplasias Pulmonares Límite: Animals / Humans Idioma: En Revista: Int J Mol Sci Año: 2023 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Carcinoma de Células Pequeñas / Carcinoma Neuroendocrino / Carcinoma de Células Grandes / Carcinoma Pulmonar de Células Pequeñas / Neoplasias Pulmonares Límite: Animals / Humans Idioma: En Revista: Int J Mol Sci Año: 2023 Tipo del documento: Article País de afiliación: España