Cancer Research Program, Department of Medicine, Research Institute of McGill University Health Center, Montreal, QC H4A 3J1, Canada.
Division of Medical Genetics, Fondazione IRCCS Casa Sollievo della Sofferenza, 71013 San Giovanni Rotondo, Italy.
Cells. 2024 Jun 4;13(11):973. doi: 10.3390/cells13110973.
Over the past few decades, the worldwide incidence of cutaneous melanoma, a malignant neoplasm arising from melanocytes, has been increasing markedly, leading to the highest rate of skin cancer-related deaths. While localized tumors are easily removed by excision surgery, late-stage metastatic melanomas are refractory to treatment and exhibit a poor prognosis. Consequently, unraveling the molecular mechanisms underlying melanoma tumorigenesis and metastasis is crucial for developing novel targeted therapies. We found that the multiple endocrine neoplasia type 1 (MEN1) gene product Menin is required for the transforming growth factor beta (TGFβ) signaling pathway to induce cell growth arrest and apoptosis in vitro and prevent tumorigenesis in vivo in preclinical xenograft models of melanoma. We further identified point mutations in two MEN1 family members affected by melanoma that led to proteasomal degradation of the MEN1 gene product and to a loss of TGFβ signaling. Interestingly, blocking the proteasome degradation pathway using an FDA-approved drug and RNAi targeting could efficiently restore MEN1 expression and TGFβ transcriptional responses. Together, these results provide new potential therapeutic strategies and patient stratification for the treatment of cutaneous melanoma.
在过去的几十年中,源自黑素细胞的恶性肿瘤——皮肤黑色素瘤的全球发病率显著增加,导致与皮肤癌相关的死亡率达到最高。虽然局部肿瘤可以通过切除术轻易切除,但晚期转移性黑色素瘤对治疗具有抗药性,预后较差。因此,揭示黑色素瘤发生和转移的分子机制对于开发新型靶向治疗至关重要。我们发现,多发性内分泌肿瘤 1 型(MEN1)基因产物 Menin 是转化生长因子β(TGFβ)信号通路所必需的,可在体外诱导细胞生长停滞和凋亡,并在黑色素瘤的临床前异种移植模型中预防肿瘤发生。我们进一步鉴定了两个受黑色素瘤影响的 MEN1 家族成员的点突变,导致 MEN1 基因产物的蛋白酶体降解,并导致 TGFβ 信号丢失。有趣的是,使用 FDA 批准的药物和 RNAi 靶向阻断蛋白酶体降解途径可以有效地恢复 MEN1 表达和 TGFβ 转录反应。总之,这些结果为治疗皮肤黑色素瘤提供了新的潜在治疗策略和患者分层。