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NTP与西妥昔单抗联合使用可抑制西妥昔单抗耐药的口腔鳞状细胞癌(OSCC)细胞的侵袭/迁移:与NF-κB信号传导有关。

Combination of NTP with cetuximab inhibited invasion/migration of cetuximab-resistant OSCC cells: Involvement of NF-κB signaling.

作者信息

Chang Jae Won, Kang Sung Un, Shin Yoo Seob, Seo Seong Jin, Kim Yeon Soo, Yang Sang Sik, Lee Jong-Soo, Moon Eunpyo, Lee Keunho, Kim Chul-Ho

机构信息

Department of Otolaryngology-Head and Neck Surgery, College of Medicine, Chungnam National University, Daejeon, Republic of Korea.

Department of Otolaryngology, School of Medicine, Ajou University, Suwon, Republic of Korea.

出版信息

Sci Rep. 2015 Dec 14;5:18208. doi: 10.1038/srep18208.

Abstract

Although the epidermal growth factor receptor (EGFR) is an established target in head-and-neck cancer (HNC), resistance to EGFR-targeted therapy mediated by various mechanisms has been reported. Therefore, a combination strategy to overcome resistance to EGFR mono-targeted therapy is clinically required. We have previously demonstrated that non-thermal atmospheric pressure plasma (NTP) induces death of various cancer cells, including oral squamous cancer (OSCC) cells. In this study, we report for the first time that combining NTP treatment with cetuximab led to inhibition of migration and invasion in cetuximab-resistant OSCC cells, which could be a promising strategy to overcome resistance to anti-EGFR therapy. NTP induced deactivation of NF-κB in SCCQLL1 cells, but not in MSKQLL1 cells. In addition, NTP increased the expression level of E-cadherin, and decreased those of vimentin, Slug, Snail, matrix metalloproteinase (MMP)-2, -9, and activities of MMPs. Moreover, NF-κB upregulation using cDNA diminished the combination effect of NTP on invasion, migration and related signals. Taken together, these results indicate that the combination of NTP with cetuximab can decrease invasiveness in cetuximab-resistant OSCCs through a novel mechanism involving the NF-κB pathway. These findings show the therapeutic potential of treatment that combines NTP and cetuximab in OSCC.

摘要

尽管表皮生长因子受体(EGFR)是头颈癌(HNC)中已确定的治疗靶点,但已有报道称,EGFR靶向治疗会因多种机制产生耐药性。因此,临床上需要一种联合策略来克服对EGFR单靶点治疗的耐药性。我们之前已经证明,非热大气压力等离子体(NTP)可诱导包括口腔鳞状细胞癌(OSCC)细胞在内的多种癌细胞死亡。在本研究中,我们首次报道,将NTP治疗与西妥昔单抗联合使用可抑制西妥昔单抗耐药的OSCC细胞的迁移和侵袭,这可能是克服抗EGFR治疗耐药性的一种有前景的策略。NTP可诱导SCCQLL1细胞中的NF-κB失活,但对MSKQLL1细胞无效。此外,NTP可增加E-钙黏蛋白的表达水平,降低波形蛋白、Slug、Snail、基质金属蛋白酶(MMP)-2、-9的表达水平以及MMP的活性。此外,使用cDNA上调NF-κB可减弱NTP对侵袭、迁移及相关信号的联合作用。综上所述,这些结果表明,NTP与西妥昔单抗联合使用可通过一种涉及NF-κB通路的新机制降低西妥昔单抗耐药的OSCC的侵袭性。这些发现显示了NTP与西妥昔单抗联合治疗在OSCC中的治疗潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7f8/4677387/8e42afb1579a/srep18208-f1.jpg

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