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학술저널
저자정보
Lara-Padilla, E (Laboratory of Molecular Oncology and Oxidative Stress, ESM, IPN) Miliar-Garcia, A (Laboratory of Molecular Biology, ESM, IPN) Gomez-Lopez, M (Laboratory of Molecular Biology, ESM, IPN) Romero-Morelos, P (Laboratory of Genomic Oncology, Medical Research Unit in Oncological Diseases, Centro Medico Nacional Siglo XXI, IMSS) Bazan-Mendez, CI (Laboratory of Cellular Biology, CINVESTAV) Alfaro-Rodriguez, A (Division of Neuroscience, INR, SSA) Anaya-Ruiz, M (Laboratory of Cellular Biology CIBIOR, IMSS) Callender, K (Cardio-Neuropthalmological and Transplant Center, Ministry of Public Health) Carlos, A (Electron Microscopy Laboratory, INR, SSA) Bandala, C (Division of Neuroscience, INR, SSA)
저널정보
아시아태평양암예방학회 Asian Pacific journal of cancer prevention : APJCP Asian Pacific journal of cancer prevention : APJCP 제17권 제4호
발행연도
2016.1
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1,967 - 1,971 (5page)

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Background: In tumor cells, aberrant differentiation programs have been described. Several neuronal proteins have been found associated with morphological neuronal-glial changes in breast cancer (BCa). These neuronal proteins have been related to mechanisms that are involved in carcinogenesis; however, this regulation is not well understood. Microtubule-associated protein-tau (MAP-Tau) has been describing in BCa but not its variants. This finding could partly explain the neuronal-glial morphology of BCa cells. Our aim was to determine mRNA expression of MAP-tau variants 2, 4 and 6 in breast cancer cell lines. Materials and Methods: Cultured cell lines MCF-10A, MDA-MB-231, SKBR3 and T47D were observed under phase-contrast microscopy for neural morphology and analyzed for gene expression of MAP-Tau transcript variants 2, 4 and 6 by real-time PCR. Results: Regarding morphology like neural/glial cells, T47D line shown more cells with these features than MDA-MB-231 and SKBR. In another hand, we found much greater mRNA expression of MAP-Tau transcript variants 2, and to a lesser extent 4 and 6, in T47D cells than the other lines. In conclusion, regulation of MAP-Tau could bring about changes in cytoskeleton, cell morphology and motility; these findings cast further light on neuronal transdifferentiation in BCa.

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