Manirakiza Felix, Rutaganda Eric, Yamada Hidetaka, Iwashita Yuji, Rugwizangoga Belson, Seminega Benoit, Dusabejambo Vincent, Ntakirutimana Gervais, Ruhangaza Deogratias, Uwineza Annette, Shinmura Kazuya, Sugimura Haruhiko
Department of Pathology, College of Medicine and Health Sciences, University of Rwanda, Kigali P.O. Box 3286, Rwanda.
Department of Pathology, University Teaching Hospital of Kigali, Kigali P.O. Box 655, Rwanda.
Curr Issues Mol Biol. 2023 May 16;45(5):4359-4374. doi: 10.3390/cimb45050277.
Cancer research in Rwanda is estimated to be less than 1% of the total African cancer research output with limited research on colorectal cancer (CRC). Rwandan patients with CRC are young, with more females being affected than males, and most patients present with advanced disease. Considering the paucity of oncological genetic studies in this population, we investigated the mutational status of CRC tissues, focusing on the , ( and genes. Our aim was to determine whether there were any differences between Rwandan patients and other populations. To do so, we performed Sanger sequencing of the DNA extracted from formalin-fixed paraffin-embedded adenocarcinoma samples from 54 patients (mean age: 60 years). Most tumors were located in the rectum (83.3%), and 92.6% of the tumors were low-grade. Most patients (70.4%) reported never smoking, and 61.1% of patients had consumed alcohol. We identified 27 variants of , including 3 novel mutations (c.4310_4319delAAACACCTCC, c.4463_4470delinsA, and c.4506_4507delT). All three novel mutations are classified as deleterious by MutationTaster2021. We found four synonymous variants (c.330C>A, c.366C>T, c.513T>C, and c.735G>A) of . For , we found six variants (Asp173, Gly13Asp, Gly12Ala, Gly12Asp, Gly12Val, and Gln61His), the last four of which are pathogenic. In conclusion, here we contribute new genetic variation data and provide clinicopathological information pertinent to CRC in Rwanda.
据估计,卢旺达的癌症研究占非洲癌症研究总量的比例不到1%,对结直肠癌(CRC)的研究有限。卢旺达的CRC患者较为年轻,女性患者多于男性,且大多数患者就诊时已处于疾病晚期。鉴于该人群肿瘤学基因研究匮乏,我们对CRC组织的突变状态进行了调查,重点关注 、 ( 和 基因。我们的目的是确定卢旺达患者与其他人群之间是否存在差异。为此,我们对从54例患者(平均年龄:60岁)的福尔马林固定石蜡包埋腺癌样本中提取的DNA进行了桑格测序。大多数肿瘤位于直肠(83.3%),92.6%的肿瘤为低级别。大多数患者(70.4%)报告从不吸烟,61.1%的患者饮酒。我们鉴定出 基因的27个变异,包括3个新突变(c.4310_4319delAAACACCTCC、c.4463_4470delinsA和c.4506_4507delT)。MutationTaster2021将所有这三个新突变归类为有害突变。我们发现了 基因的四个同义变异(c.330C>A、c.366C>T、c.513T>C和c.735G>A)。对于 基因,我们发现了六个变异(Asp173、Gly13Asp、Gly12Ala、Gly12Asp、Gly12Val和Gln61His),其中最后四个是致病的。总之,我们在此提供了新的基因变异数据,并提供了与卢旺达CRC相关的临床病理信息。