Lou Hong, Villagran Guillermo, Boland Joseph F, Im Kate M, Polo Sarita, Zhou Weiyin, Odey Ushie, Juárez-Torres Eligia, Medina-Martínez Ingrid, Roman-Basaure Edgar, Mitchell Jason, Roberson David, Sawitzke Julie, Garland Lisa, Rodríguez-Herrera Maria, Wells David, Troyer Jennifer, Pinto Francisco Castillo, Bass Sara, Zhang Xijun, Castillo Miriam, Gold Bert, Morales Hesler, Yeager Meredith, Berumen Jaime, Alvirez Enrique, Gharzouzi Eduardo, Dean Michael
Basic Science Program, Leidos Biomedical Research, Inc., Frederick, Maryland.
Instituto de Cancerologia, Guatemala City, Guatemala.
Clin Cancer Res. 2015 Dec 1;21(23):5360-70. doi: 10.1158/1078-0432.CCR-14-1837. Epub 2015 Jun 16.
Cervical cancer is one of the most common causes of cancer mortality for women living in poverty, causing more than 28,000 deaths annually in Latin America and 266,000 worldwide. To better understand the molecular basis of the disease, we ascertained blood and tumor samples from Guatemala and Venezuela and performed genomic characterization.
We performed human papillomavirus (HPV) typing and identified somatically mutated genes using exome and ultra-deep targeted sequencing with confirmation in samples from Mexico. Copy number changes were also assessed in the exome sequence.
Cervical cancer cases in Guatemala and Venezuela have an average age of diagnosis of 50 years and 5.6 children. Analysis of 675 tumors revealed activation of PIK3CA and other PI3K/AKT pathway genes in 31% of squamous carcinomas and 24% of adeno- and adenosquamous tumors, predominantly at two sites (E542K, E545K) in the helical domain of the PIK3CA gene. This distribution of PIK3CA mutations is distinct from most other cancer types and does not result in the in vitro phosphorylation of AKT. Somatic mutations were more frequent in squamous carcinomas diagnosed after the age of 50 years. Frequent gain of chromosome 3q was found, and low PIK3CA mutation fractions in many tumors suggest that PI3K mutation can be a late event in tumor progression.
PI3K pathway mutation is important to cervical carcinogenesis in Latin America. Therapeutic agents that directly target PI3K could play a role in the therapy of this common malignancy.
宫颈癌是贫困地区女性癌症死亡的最常见原因之一,在拉丁美洲每年导致超过28000人死亡,在全球范围内每年导致266000人死亡。为了更好地了解该疾病的分子基础,我们采集了危地马拉和委内瑞拉的血液及肿瘤样本,并进行了基因组特征分析。
我们进行了人乳头瘤病毒(HPV)分型,并使用外显子组和超深度靶向测序鉴定体细胞突变基因,在来自墨西哥的样本中进行了验证。还在外显子组序列中评估了拷贝数变化。
危地马拉和委内瑞拉的宫颈癌病例平均诊断年龄为50岁,平均育有5.6个子女。对675个肿瘤的分析显示,31%的鳞状细胞癌和24%的腺癌及腺鳞癌中PIK3CA和其他PI3K/AKT通路基因发生激活,主要位于PIK3CA基因螺旋结构域的两个位点(E542K、E545K)。PIK3CA突变的这种分布与大多数其他癌症类型不同,并且不会导致体外AKT磷酸化。50岁以后诊断出的鳞状细胞癌中体细胞突变更为频繁。发现3号染色体长臂频繁扩增,许多肿瘤中PIK3CA突变比例较低,这表明PI3K突变可能是肿瘤进展中的晚期事件。
PI3K通路突变对拉丁美洲宫颈癌的发生发展很重要。直接靶向PI3K的治疗药物可能在这种常见恶性肿瘤的治疗中发挥作用。