Association of TGIFLX/Y mRNA expression with prostate cancer
Prostate cancer is the most common type of solid tumor and a leading cause of cancer-related death of men living in the developed world. In recent years, the molecular mechanisms involved in prostate cancer development and/or progression have been intensely studied and several genes have been identi...
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Published in | Medical oncology (Northwood, London, England) Vol. 26; no. 1; pp. 73 - 77 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
New York
Humana Press Inc
01.03.2009
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Summary: | Prostate cancer is the most common type of solid tumor and a leading cause of cancer-related death of men living in the developed world. In recent years, the molecular mechanisms involved in prostate cancer development and/or progression have been intensely studied and several genes have been identified.
TGIFLX/Y
(
TGIFLX
and
TGIFLY
) are members of the homeobox superfamily of genes whose function(s) is unknown. To investigate
TGIFLX/Y
mRNA expression in prostate cancer, we studied two different types of clinical samples, namely 60 prostate tumors and 15 cases of benign prostate hyperplasia (BPH), by RT-PCR. Our results revealed that most prostate tumors (73.5%) express at least one of these genes, although different patterns of
TGIFLX/Y
mRNA expression were observed. In some tumor samples the expression of both genes was detected, while in others no expression of either gene was observed. Notably, there was a significant correlation between expression of both
TGIFLX
and
TGIFLY
and a Gleason score of ≥6 (
P
= 0.038). By contrast, expression of
TGIFLX/Y
mRNA in BPH samples could not be detected. These results suggest an association of
TGIFLX/Y
expression with the progression of prostate cancer. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 1357-0560 1559-131X |
DOI: | 10.1007/s12032-008-9086-7 |