Department of Biomedical Engineering, Texas A&M University, 3120 TAMU, 5016 Emerging Technologies Building, College Station, TX 77843, USA.
Dis Model Mech. 2022 May 1;15(5). doi: 10.1242/dmm.049520. Epub 2022 Jun 1.
Diverse factors contribute to significant and dire disparities in cancer risk and treatment outcomes. To address this, there was a call for inclusion of sex as a biological variable, which resulted in more instances of careful inclusion of sex in preclinical studies of cancer. Another variable in cancer treatment is genetic ancestry. Although this is considered explicitly in clinical research, it is considerably neglected in preclinical studies. Preclinical research can use several 3D in vitro model systems, such as spheroids/organoids, xenografts, or other bioengineered systems that combine biomaterials and cellular material. Ultimately, the cellular base for all of these in vitro model systems is derived from human cell lines or patient samples, to investigate mechanisms of cancer and screen novel therapeutics, all of which aim to maximize successful outcomes in clinical trials. This in itself offers an opportunity to potentiate effective treatments for many groups of people, when diverse variables like genetic ancestry are consciously included into study design. This Perspective highlights the need for conscious inclusion of genetic ancestry in preclinical cancer tissue engineering, especially when it pertains to determining therapeutic outcomes.
多种因素导致癌症风险和治疗结果存在显著而严重的差异。为了解决这个问题,有人呼吁将性别纳入生物学变量,这导致在癌症的临床前研究中更频繁地仔细纳入性别因素。癌症治疗的另一个变量是遗传背景。尽管在临床研究中明确考虑了这一点,但在临床前研究中却被严重忽视。临床前研究可以使用几种 3D 体外模型系统,如球体/类器官、异种移植物或其他结合生物材料和细胞材料的生物工程系统。最终,所有这些体外模型系统的细胞基础都源自人类细胞系或患者样本,以研究癌症的机制并筛选新的治疗方法,所有这些都旨在最大限度地提高临床试验的成功结果。当有意识地将遗传背景等多种变量纳入研究设计时,这本身为许多人群提供了增强有效治疗的机会。本观点强调了在临床前癌症组织工程中自觉纳入遗传背景的必要性,特别是在确定治疗结果时。