TY - JOUR
T1 - HtrA1 in human urothelial bladder cancer
T2 - A secreted protein and a potential novel biomarker
AU - Lorenzi, Teresa
AU - Lorenzi, Maria
AU - Altobelli, Emma
AU - Marzioni, Daniela
AU - Mensà, Emanuela
AU - Quaranta, Alexia
AU - Paolinelli, Francesca
AU - Morroni, Manrico
AU - Mazzucchelli, Roberta
AU - De Luca, Antonio
AU - Procopio, Antonio Domenico
AU - Baldi, Alfonso
AU - Muzzonigro, Giovanni
AU - Montironi, Rodolfo
AU - Castellucci, Mario
PY - 2013/12/1
Y1 - 2013/12/1
N2 - Our aim was to analyze the expression of the serine protease HtrA1 in human bladder tissue and urine in order to point out its possible association with the presence of urothelial bladder cancer. Bladder tissue and urine specimens from cancer patients with different tumor grades and stages (n = 68) and from individuals with cystitis (n = 16) were collected along with biopsy specimens and urine from healthy individuals (n = 68). For the first time, we demonstrated by immunohistochemistry that HtrA1 protein is produced by bladder urothelium in both physiological and inflammatory conditions, whereas it is not detectable in urothelial cancer cells regardless of tumor grade and stage. A different HtrA1 expression between normal-looking and neoplastic bladder tissue, despite similar HtrA1 mRNA levels, was also found by western blotting, which disclosed the presence of two forms of HtrA1, a native form of ∼50 kDa and an autocatalytic form of ∼38 kDa. Our investigations documented the presence of the two forms of HtrA1 also in urine. The ∼38 kDa form was significantly down-regulated in neoplastic tissue, whereas significantly higher amounts of both HtrA1 forms were found in urine from cancer patients compared with both healthy subjects and patients with cystitis. Our findings suggest that HtrA1 is a downexpressed molecule since an early stage of bladder urothelial carcinoma development and that urinary HtrA1 protein may be considered, if successfully validated, as an early and highly sensitive and specific biomarker for this neoplasia (the sensitivity and specificity of HtrA1 are 92.65% and 95.59%, respectively).
AB - Our aim was to analyze the expression of the serine protease HtrA1 in human bladder tissue and urine in order to point out its possible association with the presence of urothelial bladder cancer. Bladder tissue and urine specimens from cancer patients with different tumor grades and stages (n = 68) and from individuals with cystitis (n = 16) were collected along with biopsy specimens and urine from healthy individuals (n = 68). For the first time, we demonstrated by immunohistochemistry that HtrA1 protein is produced by bladder urothelium in both physiological and inflammatory conditions, whereas it is not detectable in urothelial cancer cells regardless of tumor grade and stage. A different HtrA1 expression between normal-looking and neoplastic bladder tissue, despite similar HtrA1 mRNA levels, was also found by western blotting, which disclosed the presence of two forms of HtrA1, a native form of ∼50 kDa and an autocatalytic form of ∼38 kDa. Our investigations documented the presence of the two forms of HtrA1 also in urine. The ∼38 kDa form was significantly down-regulated in neoplastic tissue, whereas significantly higher amounts of both HtrA1 forms were found in urine from cancer patients compared with both healthy subjects and patients with cystitis. Our findings suggest that HtrA1 is a downexpressed molecule since an early stage of bladder urothelial carcinoma development and that urinary HtrA1 protein may be considered, if successfully validated, as an early and highly sensitive and specific biomarker for this neoplasia (the sensitivity and specificity of HtrA1 are 92.65% and 95.59%, respectively).
KW - human urothelial bladder cancer
KW - serine protease HtrA1
KW - T24 cell lines
KW - TCC-SUP
KW - urinary biomarkers
KW - UROtsa
UR - http://www.scopus.com/inward/record.url?scp=84884904371&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84884904371&partnerID=8YFLogxK
U2 - 10.1002/ijc.28280
DO - 10.1002/ijc.28280
M3 - Article
C2 - 23712470
AN - SCOPUS:84884904371
VL - 133
SP - 2650
EP - 2661
JO - International Journal of Cancer
JF - International Journal of Cancer
SN - 0020-7136
IS - 11
ER -