Objective: p53 and androgen receptor gene changes and bcl-2 expression in prostatic intraepithetial neoplasia (PIN) and adenocarcinoma were studied. The genetic associations of PIN and adenocarcinoma as detected by FISH and immunohistochemistry were discussed. Material and Method: The study group consisted of 18 prostate cancer cases treated by radical prostatectomy. The p53 and androgen receptor gene changes ar chromosomal level were studied using the FISH technique. Also, immunohistochemistry was used to search for bcl-2 expression. Results: Of the 18 cases studied by FISH, it was found that in benign areas AR gene amplification was 78% (14/18) and 100% disomy with wild type p53, in PIN areas AR gene amplification was 33% (6/18), p53 ampl...
The activation of oncogenes and inactivation of tumor suppressor genes (TSGs) have been implicated i...
WOS: 000329790100015PubMed ID: 25536734Aim: To determine the relationship between androgen receptor ...
Objective: To interrogate enriched prostate cancer cells and autologous non-malignant prostate epith...
PURPOSE: To assess the feasibility of characterizing gene copy number alteration by fluorescence in ...
Includes bibliographical references (leaves 40-44).The aims of this study were to determine the age ...
Aim: To determine the relationship between androgen receptor (AR) gene polymorphism and prostate can...
Prostate cancer is one of the major causes of cancer-related deaths in males in Western countries. A...
TMPRSS2/ERG rearrangement, PTEN gene deletion, and androgen receptor (AR) gene amplification have be...
Small cell carcinoma of the prostate (PSCC) is a highly aggressive malignancy that often develops in...
It is possible that structural changes of the androgen receptor (AR) contribute to the insensitivity...
tate is the second most common cause of cancer deaths in men. Little is known about the pathogenesis...
The most common molecular alterations observed in prostate cancer are increased bcl-2 protein expres...
TMPRSS2/ERG rearrangement, PTEN gene deletion, and androgen receptor (AR) gene amplification have be...
OBJECTIVES: To evaluate the androgen receptor (AR) gene copy number in androgen deprivation therapy ...
The role of the current study in detecting polymorphisms in the gene P53codon72, a gene that has mor...
The activation of oncogenes and inactivation of tumor suppressor genes (TSGs) have been implicated i...
WOS: 000329790100015PubMed ID: 25536734Aim: To determine the relationship between androgen receptor ...
Objective: To interrogate enriched prostate cancer cells and autologous non-malignant prostate epith...
PURPOSE: To assess the feasibility of characterizing gene copy number alteration by fluorescence in ...
Includes bibliographical references (leaves 40-44).The aims of this study were to determine the age ...
Aim: To determine the relationship between androgen receptor (AR) gene polymorphism and prostate can...
Prostate cancer is one of the major causes of cancer-related deaths in males in Western countries. A...
TMPRSS2/ERG rearrangement, PTEN gene deletion, and androgen receptor (AR) gene amplification have be...
Small cell carcinoma of the prostate (PSCC) is a highly aggressive malignancy that often develops in...
It is possible that structural changes of the androgen receptor (AR) contribute to the insensitivity...
tate is the second most common cause of cancer deaths in men. Little is known about the pathogenesis...
The most common molecular alterations observed in prostate cancer are increased bcl-2 protein expres...
TMPRSS2/ERG rearrangement, PTEN gene deletion, and androgen receptor (AR) gene amplification have be...
OBJECTIVES: To evaluate the androgen receptor (AR) gene copy number in androgen deprivation therapy ...
The role of the current study in detecting polymorphisms in the gene P53codon72, a gene that has mor...
The activation of oncogenes and inactivation of tumor suppressor genes (TSGs) have been implicated i...
WOS: 000329790100015PubMed ID: 25536734Aim: To determine the relationship between androgen receptor ...
Objective: To interrogate enriched prostate cancer cells and autologous non-malignant prostate epith...