Rotimi Solomon O, Rotimi Oluwakemi A, Salhia Bodour
Department of Translational Genomics, Keck School of Medicine, University of Southern California, Los Angeles, CA, United States.
Department of Biochemistry, Covenant University, Ota, Nigeria.
Front Oncol. 2021 Feb 15;10:606400. doi: 10.3389/fonc.2020.606400. eCollection 2020.
Cancer is the second leading cause of death globally and is projected to overtake infectious disease as the leading cause of mortality in Africa within the next two decades. Cancer is a group of genomic diseases that presents with intra- and inter-population unique phenotypes, with Black populations having the burden of morbidity and mortality for most types. At large, the prevention and treatment of cancers have been propelled by the understanding of the genetic make-up of the disease of mostly non-African populations. By the same token, there is a wide knowledge gap in understanding the underlying genetic causes of, and genomic alterations associated with, cancer among black Africans. Accordingly, we performed a review of the literature to survey existing studies on cancer genetics/genomics and curated findings pertaining to publications across multiple cancer types conducted on African populations. We used PubMed MeSH terms to retrieve the relevant publications from 1990 to December 2019. The metadata of these publications were extracted using R text mining packages: RISmed and Pubmed.mineR. The data showed that only 0.329% of cancer publications globally were on Africa, and only 0.016% were on cancer genetics/genomics from Africa. Although the most prevalent cancers in Africa are cancers of the breast, cervix, uterus, and prostate, publications representing breast, colorectal, liver, and blood cancers were the most frequent in our review. The most frequently reported cancer genes were , , and . Next, the genes reported in the reviewed publications' abstracts were extracted and annotated into three gene ontology classes. Genes in the class were mostly associated with , while those in and classes were mainly associated with cell process, biological regulation, and binding, and catalytic activity, respectively. Overall, this review highlights the paucity of research on cancer genomics on African populations, identified gaps, and discussed the need for concerted efforts to encourage more research on cancer genomics in Africa.
癌症是全球第二大死因,预计在未来二十年内将超过传染病,成为非洲的主要死因。癌症是一组基因组疾病,呈现出群体内和群体间独特的表型,大多数类型的癌症中,黑人人群的发病率和死亡率负担最重。总体而言,对大多数非非洲人群疾病基因构成的了解推动了癌症的预防和治疗。同样,在理解非洲黑人癌症的潜在遗传原因以及与之相关的基因组改变方面,存在很大的知识差距。因此,我们对文献进行了综述,以调查关于癌症遗传学/基因组学的现有研究,并整理了针对非洲人群多种癌症类型的出版物中的研究结果。我们使用PubMed医学主题词从1990年至2019年12月检索相关出版物。这些出版物的元数据使用R文本挖掘包RISmed和Pubmed.mineR进行提取。数据显示,全球仅0.329%的癌症出版物是关于非洲的,而仅0.016%是关于非洲癌症遗传学/基因组学的。尽管非洲最常见的癌症是乳腺癌、子宫颈癌、子宫癌和前列腺癌,但在我们的综述中,代表乳腺癌、结直肠癌、肝癌和血癌的出版物最为常见。最常报道的癌症基因是 、 和 。接下来,提取了综述出版物摘要中报道的基因,并注释为三个基因本体类别。 类中的基因大多与 相关,而 类和 类中的基因分别主要与细胞过程、生物调节和结合以及催化活性相关。总体而言,本综述强调了非洲人群癌症基因组学研究的匮乏,指出了差距,并讨论了需要共同努力鼓励在非洲开展更多癌症基因组学研究。