4.6 Article

Expression of Luteinizing Hormone-Releasing Hormone (LHRH) and Type-I LHRH Receptor in Transitional Cell Carcinoma Type of Human Bladder Cancer

期刊

MOLECULES
卷 26, 期 5, 页码 -

出版社

MDPI
DOI: 10.3390/molecules26051253

关键词

LHRH receptor; targeted therapy; bladder cancer; radioligand binding assay; immunohistochemistry; Western Blot; RT-PCR

资金

  1. Ministry for Innovation and Technology in Hungary [GINOP-2.3.2-15-2016-00043, TKP2020-IKA-04]
  2. European Union
  3. European Regional Development Fund

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This study investigates the expression of LHRH and LHRH-R-I in transitional cell carcinoma (TCC) type of human bladder cancer, finding high incidence of expression of both in the samples examined. Positive immunostaining for LHRH-R-I with different expression intensity was found in all samples, showing a negative correlation with TCC grade.
Bladder cancer (BC) is the tenth most frequently detected cancer in both sexes. Type-I luteinizing hormone-releasing hormone (LHRH) receptor (LHRH-R-I) is expressed not only in the pituitary, but also in several types of cancer disease. There are few data about LHRH-R-I expression in human BC. This study aimed to investigate the expression of LHRH and LHRH-R-I in the transitional cell carcinoma (TCC) type of human BC. RNA was extracted from 24 human bladder tumor specimens and three BC cell lines. RT-PCR was performed to detect mRNA for LHRH and LHRH-R-I. The protein of LHRH-R-I was further studied by immunohistochemistry (IHC), ligand competition assay, and Western Blot. PCR products of LHRH were found in 19 of 24 (79%) specimens and mRNA of LHRH-R-I was detected in 20 of 24 specimens (83%). Positive immunostaining for LHRH-R-I with different expression intensity was found in all samples examined, showing negative correlation with TCC grade. Radioligand binding studies also showed the presence of specific LHRH-R-I and high affinity binding of LHRH analogs. The high incidence of LHRH-R in BC suggests that it could serve as a molecular target for therapy of human BC with cytotoxic LHRH analogs or modern powerful antagonistic analogs of LHRH.

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