TY - JOUR
T1 - Human collagen XV is a prominent histopathological component of sinusoidal capillarization in hepatocellular carcinogenesis
AU - Kimura, Kouji
AU - Nakayama, Masaru
AU - Naito, Ichiro
AU - Komiyama, Takaaki
AU - Ichimura, Kouichi
AU - Asano, Hiroaki
AU - Tsukuda, Kazunori
AU - Ohtsuka, Aiji
AU - Oohashi, Toshitaka
AU - Miyoshi, Shinichiro
AU - Ninomiya, Yoshifumi
N1 - Funding Information:
This work was supported by a Grant-in-Aid for Challenging Exploratory Research (No. 24659590) to Yoshifumi Ninomiya from the Ministry of Education, Culture, Sports, Science, and Technology (MEXT) of Japan and the research grant for researching digestive diseases to Kazunori Tsukuda from Merck Serono (Tokyo, Japan). We thank Dr. Francesco Ramirez for critical reading of the manuscript, Dr. Hiroyuki Yanai for pathological advice, and Ms. Yumiko Morishita for assistance with immunohistochemical analysis. This work is dedicated to the memory of Prof. Yoshifumi Ninomiya.
Publisher Copyright:
© 2015, Japan Society of Clinical Oncology.
PY - 2016/4/1
Y1 - 2016/4/1
N2 - Background: Increased expression of collagen XV has been reported in hepatocellular carcinogenesis in mice. The aim of this study was to confirm the previous murine findings in human hepatocellular carcinoma (HCC) specimens, along with the histopathological distribution of collagen XV in tumoral tissues. Methods: Sixty-three primary HCC specimens were examined. Immunostaining of collagen XV and quantitative reverse transcriptional PCR of COL15A1, which encodes collagen XV, were performed. Results: Positive staining of collagen XV was observed in all tumoral regions, regardless of differentiation level or pathological type of HCC, along the sinusoid-like endothelium, whereas collagen XV was not expressed in any non-tumoral region. The intensity score of collagen XV immunostaining and the mRNA value of COL15A1 were significantly correlated. COL15A1 expression in tumors was 3.24-fold higher than in non-tumoral regions. Multivariate analysis showed that COL15A1 expression was significantly higher in the absence of hepatitis virus and moderately differentiated HCC. Conclusions: COL15A1 mRNA was up-regulated in HCC and collagen XV was expressed along the sinusoid-like endothelium of HCC but not in non-tumoral regions, which implies that collagen XV contributes to the capillarization of HCC.
AB - Background: Increased expression of collagen XV has been reported in hepatocellular carcinogenesis in mice. The aim of this study was to confirm the previous murine findings in human hepatocellular carcinoma (HCC) specimens, along with the histopathological distribution of collagen XV in tumoral tissues. Methods: Sixty-three primary HCC specimens were examined. Immunostaining of collagen XV and quantitative reverse transcriptional PCR of COL15A1, which encodes collagen XV, were performed. Results: Positive staining of collagen XV was observed in all tumoral regions, regardless of differentiation level or pathological type of HCC, along the sinusoid-like endothelium, whereas collagen XV was not expressed in any non-tumoral region. The intensity score of collagen XV immunostaining and the mRNA value of COL15A1 were significantly correlated. COL15A1 expression in tumors was 3.24-fold higher than in non-tumoral regions. Multivariate analysis showed that COL15A1 expression was significantly higher in the absence of hepatitis virus and moderately differentiated HCC. Conclusions: COL15A1 mRNA was up-regulated in HCC and collagen XV was expressed along the sinusoid-like endothelium of HCC but not in non-tumoral regions, which implies that collagen XV contributes to the capillarization of HCC.
KW - Basement membrane
KW - Capillarization
KW - Collagen XV
KW - Fenestrated capillary endothelium
KW - Hepatocellular carcinoma
KW - Liver sinusoid
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U2 - 10.1007/s10147-015-0888-2
DO - 10.1007/s10147-015-0888-2
M3 - Article
C2 - 26293333
AN - SCOPUS:84939634611
SN - 1341-9625
VL - 21
SP - 302
EP - 309
JO - International Journal of Clinical Oncology
JF - International Journal of Clinical Oncology
IS - 2
ER -