Tsukamoto Shuichi, Koma Yu-Ichiro, Kitamura Yu, Tanigawa Kohei, Azumi Yuki, Miyako Shoji, Urakami Satoshi, Hosono Masayoshi, Kodama Takayuki, Nishio Mari, Shigeoka Manabu, Yokozaki Hiroshi
Division of Pathology, Department of Pathology, Kobe University Graduate School of Medicine, Kobe 650-0017, Japan.
Division of Gastro-Intestinal Surgery, Department of Surgery, Kobe University Graduate School of Medicine, Kobe 650-0017, Japan.
Cancers (Basel). 2023 May 30;15(11):2987. doi: 10.3390/cancers15112987.
Tumor-associated macrophages (TAMs) contribute to disease progression in various cancers, including esophageal squamous cell carcinoma (ESCC). We have previously used an indirect co-culture system between ESCC cell lines and macrophages to analyze their interactions. Recently, we established a direct co-culture system to closely simulate actual ESCC cell-TAM contact. We found that matrix metalloproteinase 9 (MMP9) was induced in ESCC cells by direct co-culture with TAMs, not by indirect co-culture. MMP9 was associated with ESCC cell migration and invasion, and its expression was controlled by the Stat3 signaling pathway in vitro. Immunohistochemical analyses revealed that MMP9 expression in cancer cells at the invasive front ("cancer cell MMP9") was related to high infiltration of CD204 positive M2-like TAMs ( < 0.001) and was associated with worse overall and disease-free survival of patients ( = 0.036 and = 0.038, respectively). Furthermore, cancer cell MMP9 was an independent prognostic factor for disease-free survival. Notably, MMP9 expression in cancer stroma was not associated with any clinicopathological factors or patient prognoses. Our results suggest that close interaction with TAMs infiltrating in cancer stroma or cancer nests induces MMP9 expression in ESCC cells, equipping them with more malignant features.
肿瘤相关巨噬细胞(TAM)在包括食管鳞状细胞癌(ESCC)在内的多种癌症中促进疾病进展。我们之前使用ESCC细胞系与巨噬细胞之间的间接共培养系统来分析它们之间的相互作用。最近,我们建立了一种直接共培养系统,以密切模拟实际的ESCC细胞与TAM接触。我们发现,与TAM直接共培养而非间接共培养可诱导ESCC细胞中基质金属蛋白酶9(MMP9)的产生。MMP9与ESCC细胞迁移和侵袭相关,其表达在体外受Stat3信号通路控制。免疫组织化学分析显示,侵袭前沿癌细胞中的MMP9表达(“癌细胞MMP9”)与CD204阳性M2样TAM的高浸润相关(<0.001),并且与患者较差的总生存期和无病生存期相关(分别为=0.036和=0.038)。此外,癌细胞MMP9是无病生存期的独立预后因素。值得注意的是,癌基质中的MMP9表达与任何临床病理因素或患者预后均无关。我们的结果表明,与浸润在癌基质或癌巢中的TAM密切相互作用可诱导ESCC细胞中MMP9表达,使其具有更多恶性特征。