类有机物
间质细胞
基质
基底膜
胰腺癌
基质金属蛋白酶
MMP2型
肝星状细胞
癌症研究
病理
生物
化学
转移
细胞生物学
医学
癌症
免疫组织化学
生物化学
遗传学
作者
Kazuhiro Koikawa,Kenoki Ohuchida,Yukio Ando,Shin Kibe,Hiromichi Nakayama,Shin Takesue,Sho Endo,Toshiya Abe,Takashi Okumura,Chika Iwamoto,Taiki Moriyama,Kohei Nakata,Yoshihiro Miyasaka,Takao Ohtsuka,Eishi Nagai,Kazuhiro Mizumoto,Makoto Hashizume,Masafumi Nakamura
出处
期刊:Cancer Letters
[Elsevier BV]
日期:2018-03-23
卷期号:425: 65-77
被引量:66
标识
DOI:10.1016/j.canlet.2018.03.031
摘要
Stroma invasion is an important step in pancreatic cancer progression. However, how pancreatic ductal adenocarcinoma (PDAC) with ductal structure invades the surrounding stroma has not been clear. Here, we elucidated the mechanism of stromal invasion of PDAC, using organoids. From resected PDAC specimens, we established human PDAC organoids, which developed ductal and basement membrane (BM) structures. When the organoids were co-cultured with pancreatic stellate cells (PSCs) in a collagen matrix, organoids lost their BM and ductal structures, and invaded collagen matrix more frequently than did mono-cultured organoids. Interestingly, direct contact by PSCs to PDAC organoids was observed before BM destruction. Matrix metalloproteinase (MMP) 2 or membrane type-1 MMP (MT1MMP) knockdown in PSCs significantly attenuated BM destruction by PSCs, and retained the ductal structures in organoids. Our results imply that direct contact by PSCs induces BM destruction and stromal invasion of PDAC via MMP2 which binds to MT1MMP on PSCs.
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