Bluestone Center for Clinical Research, New York University College of Dentistry, New York, NY, United States.
Doctor of Dental Surgery Program, New York University College of Dentistry, New York, NY, United States.
Pain. 2020 Oct;161(10):2330-2343. doi: 10.1097/j.pain.0000000000001926.
Cancer cells secrete pronociceptive mediators that sensitize adjacent sensory neurons and cause pain. Identification and characterization of these mediators could pinpoint novel targets for cancer pain treatment. In this study, we identified candidate genes in cancer cell lines that encode for secreted or cell surface proteins that may drive nociception. To undertake this work, we used an acute cancer pain mouse model, transcriptomic analysis of publicly available human tumor-derived cell line data, and a literature review. Cancer cell line supernatants were assigned a phenotype based on evoked nociceptive behavior in an acute cancer pain mouse model. We compared gene expression data from nociceptive and nonnociceptive cell lines. Our analyses revealed differentially expressed genes and pathways; many of the identified genes were not previously associated with cancer pain signaling. Epidermal growth factor receptor (EGFR) and disintegrin metalloprotease domain 17 (ADAM17) were identified as potential targets among the differentially expressed genes. We found that the nociceptive cell lines contained significantly more ADAM17 protein in the cell culture supernatant compared to nonnociceptive cell lines. Cytoplasmic EGFR was present in almost all (>90%) tongue primary afferent neurons in mice. Monoclonal antibody against EGFR, cetuximab, inhibited cell line supernatant-induced nociceptive behavior in an acute oral cancer pain mouse model. We infer from these data that ADAM17-EGFR signaling is involved in cancer mediator-induced nociception. The differentially expressed genes and their secreted protein products may serve as candidate therapeutic targets for oral cancer pain and warrant further evaluation.
癌细胞分泌敏化邻近感觉神经元并引起疼痛的伤害性介质。鉴定和描述这些介质可以确定癌症疼痛治疗的新靶点。在这项研究中,我们鉴定了癌细胞系中编码分泌或细胞表面蛋白的候选基因,这些蛋白可能驱动伤害感受。为了开展这项工作,我们使用了急性癌症疼痛小鼠模型、公开可用的人类肿瘤衍生细胞系数据的转录组分析和文献综述。根据急性癌症疼痛小鼠模型中诱发的伤害性行为,将癌细胞系上清液分配给表型。我们比较了伤害感受和非伤害感受细胞系的基因表达数据。我们的分析揭示了差异表达的基因和途径;许多鉴定出的基因以前与癌症疼痛信号没有关联。表皮生长因子受体 (EGFR) 和金属蛋白酶结构域 17 (ADAM17) 被确定为差异表达基因中的潜在靶点。我们发现,与非伤害感受细胞系相比,伤害感受细胞系的细胞培养上清液中 ADAM17 蛋白含量明显更多。细胞质 EGFR 存在于小鼠几乎所有 (>90%)舌初级传入神经元中。针对 EGFR 的单克隆抗体西妥昔单抗抑制了急性口腔癌疼痛小鼠模型中细胞系上清液诱导的伤害性行为。我们从这些数据推断 ADAM17-EGFR 信号参与了癌症介质诱导的伤害感受。差异表达的基因及其分泌的蛋白产物可能作为口腔癌疼痛的候选治疗靶点,并值得进一步评估。