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P‐Glycoprotein Is Positively Correlated with p53 Protein Accumulation in Human Colorectal Cancers

To explore the relationship between mutant p53 and Pgp expression, we have examined the levels of both proteins in human colorectal adenocarcinomas. Serial frozen sections of 40 surgical samples were stained with an anti‐Pgp (MRK16) and two different anti‐p53 protein antibodies (Abs), PAb421 and Pab...

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Detalles Bibliográficos
Autores principales: Oka, Mikio, Kounoura, Kiyoshi, Narasaki, Fumihiko, Sakamoto, Akira, Fukuda, Minoru, Matsuo, Isao, Ikeda, Koki, Tsurutani, Junji, Ikuno, Nobuhiro, Omagari, Katsuhisa, Mizuta, Yohei, Soda, Hiroshi, Gudas, Jean M., Kohno, Shigeru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1997
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5921503/
https://www.ncbi.nlm.nih.gov/pubmed/9330605
http://dx.doi.org/10.1111/j.1349-7006.1997.tb00445.x
Descripción
Sumario:To explore the relationship between mutant p53 and Pgp expression, we have examined the levels of both proteins in human colorectal adenocarcinomas. Serial frozen sections of 40 surgical samples were stained with an anti‐Pgp (MRK16) and two different anti‐p53 protein antibodies (Abs), PAb421 and Pabl80l. Nineteen (47.5%) of 40 samples examined were positive for Pgp, and 18 (45%) of 40 were positive for p53. The samples that stained positively with PAb421 also stained positively with Pahl80l. Pgp expression was detected in 13 (76.5%) of 17 samples that were positive for p53 using PAb421 and in 15 (83.3%) of 18 samples that were positive for p53 using Pabl80. Thus, we found that p53 and Pgp were co‐expressed in a significant number of samples (P< 0.002). There was no relationship between Pgp or p53 protein accumulation and histologic grade or stage. The present results demonstrate that Pgp expression is closely associated with p53 protein accumulation in human colorectal cancers. These data provide evidence to support the idea that mutant p53 activates the MDR1 gene in vivo.