Wufuer Reziwan, Ma Hai-Xiu, Luo Meng-Yu, Xu Kai-Yue, Kang Ling
School of Public Health, Xinjiang Medical University, 393 Xinyi Road, Urumqi, Xinjiang Uygur Autonomous Region, 10760, China.
School of Public Health, Xinjiang Medical University, 393 Xinyi Road, Urumqi, Xinjiang Uygur Autonomous Region, 10760, China.
Photodiagnosis Photodyn Ther. 2021 Mar;33:102143. doi: 10.1016/j.pdpdt.2020.102143. Epub 2020 Dec 8.
Colorectal cancer is one of the most common gastrointestinal malignancies. Photodynamic therapy (PDT) is a novel and non-invasive treatment for tumors as PDT features small trauma, good applicability, andaccurate targeting. PDT may also be a potential treatment for colon cancer as itmay may induce suppressive effects on metastatic potential.. However, the molecular mechanism of the Chlorin e6 Photodynamic therapy (Ce6-PDT) inhibiting the migration of human colon cancer SW620 cells remains unclear.
Scratch wound healing assay, scanning electron microscope, MTT, immunofluorescence and laser confocal technique were used to investigate the suppressive effects of Ce6-PDT on the SW620 cells migration, pseudopodia, viability and the actin cytoskeleton. The effect of Ce6-PDT on actin-Filaments and signaling molecules of the Rac1/PAK1/LIMK1/cofilin signaling pathway in SW620 cells were examined by western blot analysis. RNA interference (RNAi) technology was used to establish siRNA-Rac1/SW620 cells. The combined effects of Ce6-PDT and RNAi on colon cancer SW620 cells was investigated by the same technology and methods mentioned above to clarify the signal transduction effect of Rac1/PAK1/LIMK1/cofilin signaling pathway in Ce6-PDT caused inhibition of SW620 cell migration.
The healing and migration rate of the SW620 cells was significantly reduced and the cell pseudopodia were reduced or disappeared by Ce6-PDT. The Immunofluorescence and western blot analysis results showed that Ce6-PDT destroy microfilament's original structure and significantly downregulated F-actin protein expression. The Rac1/PAK1/LIMK1/cofilin signaling pathway was downregulated by Ce6-PDT. Furthermore, the RNAi significantly strengthened the effect of Ce6-PDT on colon cancer SW620 cells migration.
Actin cytoskeleton and protrusions of SW620 cells correlate with its migration ability. Ce6-PDT suppresses SW620 cells migration by downregulating the Rac1/PAK1/LIMK1/cofilin signaling pathway, and its suppressive effect was enhanced by knocking down Rac1 gene expression.
结直肠癌是最常见的胃肠道恶性肿瘤之一。光动力疗法(PDT)是一种新型的肿瘤非侵入性治疗方法,具有创伤小、适用性好、靶向性精确等特点。PDT对结肠癌可能也具有潜在治疗作用,因为它可能对转移潜能产生抑制作用。然而,二氢卟吩e6光动力疗法(Ce6-PDT)抑制人结肠癌SW620细胞迁移的分子机制尚不清楚。
采用划痕伤口愈合试验、扫描电子显微镜、MTT法、免疫荧光和激光共聚焦技术,研究Ce6-PDT对SW620细胞迁移、伪足、活力及肌动蛋白细胞骨架的抑制作用。通过蛋白质免疫印迹分析检测Ce6-PDT对SW620细胞中肌动蛋白丝及Rac1/PAK1/LIMK1/丝切蛋白信号通路信号分子的影响。利用RNA干扰(RNAi)技术构建siRNA-Rac1/SW620细胞。采用上述相同技术和方法研究Ce6-PDT与RNAi联合作用对结肠癌SW620细胞的影响,以阐明Rac1/PAK1/LIMK1/丝切蛋白信号通路在Ce6-PDT抑制SW620细胞迁移中的信号转导作用。
Ce6-PDT显著降低SW620细胞的愈合和迁移率,细胞伪足减少或消失。免疫荧光和蛋白质免疫印迹分析结果显示,Ce6-PDT破坏微丝的原始结构,显著下调F-肌动蛋白蛋白表达。Ce6-PDT使Rac1/PAK1/LIMK1/丝切蛋白信号通路下调。此外,RNAi显著增强了Ce6-PDT对结肠癌SW620细胞迁移的作用。
SW620细胞的肌动蛋白细胞骨架和突起与其迁移能力相关。Ce6-PDT通过下调Rac1/PAK1/LIMK1/丝切蛋白信号通路抑制SW620细胞迁移,敲低Rac1基因表达可增强其抑制作用。