Kaneyoshi T, Nakatsukasa H, Higashi T, Fujiwara K, Naito I, Nouso K, Kariyama K, Kobayashi Y, Uemura M, Nakamura S I, Iwasaki Y, Tsuji T
Department of Medicine and Medical Science, Okayama University Graduate School of Medicine and Dentistry, 2-5-1 Shikata-cho, Okayama 700-8558, Japan.
Clin Cancer Res. 2001 Dec;7(12):4027-32.
The matrix-degrading proteinases are believed to play an important role in the invasion and metastasis of hepatocellular carcinoma (HCC), but no one has ever seen the in situ matrix-degrading activity in HCCs.
To demonstrate the cellular localization of actual gelatinolytic activity and to investigate the invasive potential of human HCC.
HCC cases (30) were subjected to in situ gelatin zymography and SDS-gelatin gel zymogram.
In situ gelatin zymography revealed a heterogeneous gelatinolytic activity in HCC cells, as well as stromal cells of noncancerous livers. The gelatinolytic intensity was stronger in 15 HCC nodules than in the corresponding noncancerous livers and was significantly associated with the cancer invasion to the capsule of the HCCs and to the portal veins. An intense gelatinolytic activity was detected in HCC cells in the front of tumor invasion. SDS-gelatin gel zymogram revealed gelatinases A and B that were mostly in latent forms.
The present study demonstrates high gelatinolytic activity at the invasive front of HCCs at a cellular level and that HCC has an invasive potential with the gelatin (matrix)-degrading metalloproteinases. Furthermore, it suggests the importance of the activation mechanism of gelatinolytic enzymes in the invasion and metastasis of HCCs.
基质降解蛋白酶被认为在肝细胞癌(HCC)的侵袭和转移中起重要作用,但从未有人在HCC中观察到原位基质降解活性。
证明实际明胶酶解活性的细胞定位,并研究人HCC的侵袭潜能。
对30例HCC病例进行原位明胶酶谱分析和SDS-明胶凝胶酶谱分析。
原位明胶酶谱分析显示HCC细胞以及非癌肝脏的基质细胞中存在异质性明胶酶解活性。15个HCC结节中的明胶酶解强度比相应的非癌肝脏更强,并且与HCC向包膜和门静脉的癌侵袭显著相关。在肿瘤侵袭前沿的HCC细胞中检测到强烈的明胶酶解活性。SDS-明胶凝胶酶谱分析显示明胶酶A和B大多处于潜伏形式。
本研究在细胞水平上证明了HCC侵袭前沿具有高明胶酶解活性,并且HCC具有通过明胶(基质)降解金属蛋白酶的侵袭潜能。此外,这表明明胶酶解酶的激活机制在HCC侵袭和转移中的重要性。