Department of Oral & Maxillofacial Surgery, Loma Linda University School of Dentistry, Loma Linda, CA, 92350, USA.
Department of Oral & Maxillofacial Surgery, New York University College of Dentistry, New York, NY, 10010, USA.
Adv Biol (Weinh). 2022 Sep;6(9):e2200190. doi: 10.1002/adbi.202200190. Epub 2022 Aug 4.
Oral squamous cell carcinoma (OSCC) patients suffer from poor survival due to metastasis or locoregional recurrence, processes that are both facilitated by perineural invasion (PNI). OSCC has higher rates of PNI than other cancer subtypes, with PNI present in 80% of tumors. Despite the impact of PNI on oral cancer prognosis and pain, little is known about the genes that drive PNI, which in turn drive pain, invasion, and metastasis. In this study, clinical data, preclinical, and in vitro models are leveraged to elucidate the role of neurotrophins in OSCC metastasis, PNI, and pain. The expression data in OSCC patients with metastasis, PNI, or pain demonstrate dysregulation of neurotrophin genes. TrkA and nerve growth factor receptor (NGFR) are focused, two receptors that are activated by NGF, a neurotrophin expressed at high levels in OSCC. It is demonstrated that targeted knockdown of these two receptors inhibits proliferation and invasion in an in vitro and preclinical model of OSCC, and metastasis, PNI, and pain. It is further determined that TrkA knockdown alone inhibits thermal hyperalgesia, whereas NGFR knockdown alone inhibits mechanical allodynia. Collectively the results highlight the ability of OSCC to co-opt different components of the neurotrophin pathway in metastasis, PNI, and pain.
口腔鳞状细胞癌(OSCC)患者由于转移或局部区域复发而生存状况不佳,这一过程均由神经周围侵犯(PNI)促进。OSCC 的 PNI 发生率高于其他癌症亚型,80%的肿瘤存在 PNI。尽管 PNI 对口腔癌的预后和疼痛有影响,但对于驱动 PNI 进而驱动疼痛、侵袭和转移的基因知之甚少。在这项研究中,利用临床数据、临床前和体外模型来阐明神经营养因子在 OSCC 转移、PNI 和疼痛中的作用。具有转移、PNI 或疼痛的 OSCC 患者的表达数据表明神经营养因子基因失调。TrkA 和神经生长因子受体(NGFR)是两个被神经营养因子激活的受体,在 OSCC 中高表达。研究表明,这两个受体的靶向敲低可抑制体外和临床前 OSCC 模型中的增殖和侵袭,以及转移、PNI 和疼痛。进一步确定,单独敲低 TrkA 可抑制热痛觉过敏,而单独敲低 NGFR 可抑制机械性痛觉过敏。总的来说,这些结果强调了 OSCC 能够在转移、PNI 和疼痛中共同利用神经营养因子途径的不同成分。