Hisaka T, Yano H, Haramaki M, Utsunomiya I, Kojiro M
Department of Pathology, Kurume University School of Medicine, Kurume, Fukuoka 830-0011, Japan.
Int J Oncol. 1999 Mar;14(3):453-60. doi: 10.3892/ijo.14.3.453.
In 6 HCC cell lines, clear expressions of EGFR and TGF-alpha were found in flow cytometry, while expressions of EGF, HB-EGF and AR were quite low. TGF-alpha secretion into culture supernatants became measurable when TPA 0.5 microM was added. TPA accelerated the proliferation of KYN-3 cells, and anti-TGF-alpha neutralizing antibody suppressed this proliferation in a dose-dependent manner. Addition of exogenous TGF-alpha, EGF, AR, or HB-EGF with heparin accelerated cell proliferation. In non-stimulated cultures, cell proliferation was suppressed by anti-EGFR neutralizing antibody, but not by the antibodies for EGF, TGF-alpha, AR and HB-EGF. HCC may possess a paracrine system regulated by these 4 ligands, and an autocrine system, under a certain condition, via TGF-alpha and EGFR.
在6种肝癌细胞系中,流式细胞术检测发现表皮生长因子受体(EGFR)和转化生长因子α(TGF-α)表达明显,而表皮生长因子(EGF)、肝素结合表皮生长因子(HB-EGF)和雄激素受体(AR)表达相当低。添加0.5微摩尔/升佛波酯(TPA)后,可检测到培养上清液中有TGF-α分泌。TPA加速了KYN-3细胞的增殖,抗TGF-α中和抗体以剂量依赖方式抑制了这种增殖。添加外源性TGF-α、EGF、AR或带肝素的HB-EGF可加速细胞增殖。在未刺激的培养物中,抗EGFR中和抗体可抑制细胞增殖,但抗EGF、TGF-α、AR和HB-EGF抗体则无此作用。肝癌可能拥有一个由这4种配体调控的旁分泌系统,以及在一定条件下通过TGF-α和EGFR的自分泌系统。