Genomics Unit, Keio Cancer Center, Keio University School of Medicine, 35 Shinanomachi, Shinjukuku, Tokyo, 160-8582, Japan.
Department of Obstetrics and Gynecology, Kumagaya General Hospital, Saitama, 360-8657, Japan.
Diagn Pathol. 2020 May 28;15(1):64. doi: 10.1186/s13000-020-00976-2.
Bartholin gland carcinomas (BGCs) are rare tumor types, for which no molecular analyses including genomic sequencing have been reported to date. Adenoid cystic carcinomas (ACCs) of the Bartholin's glands are an atypical histological type of BGC, and currently nothing is known regarding their genetic profiles or similarity to ACC carcinogenesis in other organs including the salivary glands, thereby limiting possible therapeutic options using precision medicine.
We used targeted gene sequencing to analyze the occurrence of 160 cancer-related genes in two patients with BG-ACC. KRAS and KDM6A mutations were detected in tumor samples collected from each patient. No KRAS mutations have been previously reported in salivary gland ACCs, indicating that the carcinogenesis of BG-ACC differs from that of the salivary gland ACCs. KDM6A mutations are often reported in salivary gland ACCs and facilitate novel gene-targeted therapy, including the use of BET and HDAC inhibitors.
A better understanding of the underlying genetic mechanisms will help to clarify the carcinogenesis of BG-ACC. In turn, this will enable treatment with novel targeting agents, as well as the initial exploration of gene-based precision oncological therapies, which aim to improve treatment outcomes for patients with this disease.
巴氏腺腺癌(BGC)是一种罕见的肿瘤类型,迄今为止,尚无包括基因组测序在内的分子分析报告。巴氏腺的腺样囊性癌(ACC)是 BGC 的一种非典型组织学类型,目前尚不清楚其遗传特征,也不清楚与唾液腺等其他器官的 ACC 发生的相似性,从而限制了使用精准医学的可能治疗选择。
我们使用靶向基因测序分析了两名 BGC-ACC 患者的 160 个癌症相关基因的发生情况。从每位患者的肿瘤样本中检测到 KRAS 和 KDM6A 突变。以前在唾液腺 ACC 中没有报道过 KRAS 突变,这表明 BGC-ACC 的发生与唾液腺 ACC 不同。KDM6A 突变经常在唾液腺 ACC 中报道,并促进新的基因靶向治疗,包括使用 BET 和 HDAC 抑制剂。
更好地了解潜在的遗传机制将有助于阐明 BGC-ACC 的发生机制。反过来,这将有助于使用新型靶向药物进行治疗,并初步探索基于基因的精准肿瘤治疗方法,旨在改善此类疾病患者的治疗效果。