Doi Takefumi, Ogawa Hiroyuki, Tanaka Yugo, Hayashi Yoshitake, Maniwa Yoshimasa
Division of Thoracic Surgery, Kobe University Graduate School of Medicine, Kobe, Hyogo 650-0017, Japan.
Department of Thoracic Surgery, Hyogo Cancer Center, Akashi, Hyogo 673-8558, Japan.
Oncol Lett. 2020 Dec;20(6):362. doi: 10.3892/ol.2020.12226. Epub 2020 Oct 14.
Invasion has a significant role in cancer progression, including expansion to surrounding tissue and metastasis. Previously, we assessed the invasive ability of cancer cells using an easy-to-prepare double-layered collagen gel hemisphere (DL-CGH) method by which cancer cell invasion can be easily visualized. The present study examined multiple lung adenocarcinoma and malignant pleural mesothelioma (MPM) cell lines using the DL-CGH method and identified inherently invasive cell lines. Next, by comparing gene expression between invasive and non-invasive cells by cDNA microarray, the potential candidate gene brain-expressed x-linked protein 1 () was identified to be involved in cancer invasion, as it was highly expressed in the invasive cell lines. Downregulation of suppressed the invasion and proliferation of the invasive tumor cell lines. The findings of the present study suggested that may promote metastasis and could be a potential oncogene and molecular therapeutic target in lung adenocarcinoma and MPM.
侵袭在癌症进展中起着重要作用,包括向周围组织扩展和转移。此前,我们使用易于制备的双层胶原凝胶半球(DL-CGH)方法评估癌细胞的侵袭能力,通过该方法可以轻松观察到癌细胞的侵袭情况。本研究使用DL-CGH方法检测了多种肺腺癌和恶性胸膜间皮瘤(MPM)细胞系,并鉴定出具有固有侵袭能力的细胞系。接下来,通过cDNA微阵列比较侵袭性细胞和非侵袭性细胞之间的基因表达,发现潜在的候选基因脑表达X连锁蛋白1()与癌症侵袭有关,因为它在侵袭性细胞系中高表达。的下调抑制了侵袭性肿瘤细胞系的侵袭和增殖。本研究结果表明,可能促进转移,并且可能是肺腺癌和MPM中的潜在癌基因和分子治疗靶点。