Department of Biomedical Engineering, University of Michigan, Ann Arbor, MI 48109, United States.
Department of Internal Medicine, Division of Pulmonary, Critical Care and Sleep Medicine, The Ohio State University Wexner College of Medicine, Columbus, OH 43210, United States.
Acta Biomater. 2022 Jul 1;146:222-234. doi: 10.1016/j.actbio.2022.04.039. Epub 2022 Apr 27.
Epithelial ovarian cancers are among the most aggressive forms of gynecological malignancies. Despite the advent of poly adenosine diphosphate-ribose polymerase (PARP) and checkpoint inhibitors, improvement to patient survival has been modest. Limited in part by clinical translation, beneficial therapeutic strategies remain elusive in ovarian cancers. Although elevated levels of extracellular proteins, including collagens, proteoglycans, and glycoproteins, have been linked to chemoresistance, they are often missing from the processes of drug- development and screening. Biophysical and biochemical signaling from the extracellular matrix (ECM) determine cellular phenotype and affect both tumor progression and therapeutic response. However, many state-of-the-art tumor models fail to mimic the complexities of the tumor microenvironment (TME) and omit key signaling components. In this article, two interpenetrating network (IPN) hydrogel scaffold platforms, comprising of alginate-collagen or agarose-collagen, have been characterized for use as 3D in vitro models of epithelial ovarian cancer ECM. These highly tunable, injection mold compatible, and inexpensive IPNs replicate the critical governing physical and chemical signaling present within the ovarian TME. Additionally, an effective and cell-friendly live-cell retrieval method has been established to recover cells post-encapsulation. Lastly, functional mechanotransduction in ovarian cancers was demonstrated by increasing scaffold stiffness within the 3D in vitro ECM models. With these features, the agarose-collagen and alginate-collagen hydrogels provide a robust TME for the study of mechanobiology in epithelial cancers. STATEMENT OF SIGNIFICANCE: Ovarian cancer is the most lethal gynecologic cancer afflicting women today. Here we present the development, characterization, and validation of 3D interpenetrating platforms to shift the paradigm in standard in vitro modeling. These models help elucidate the roles of biophysical and biochemical cues in ovarian cancer progression. The agarose-collagen and alginate-collagen interpenetrating network (IPN) hydrogels are simple to fabricate, inexpensive, and can be modified to create custom mechanical stiffnesses and concentrations of bio-adhesive motifs. Given that investigations into the roles of biophysical characteristics in ovarian cancers have provided incongruent results, we believe that the IPN platforms will be critically important to uncovering molecular drivers. We also expect these platforms to be broadly applicable to studies involving mechanobiology in solid tumors.
上皮性卵巢癌是妇科恶性肿瘤中最具侵袭性的一种。尽管多聚腺苷二磷酸核糖聚合酶(PARP)和检查点抑制剂的出现,患者的生存率仍有所提高。部分原因是临床转化受限,卵巢癌的有益治疗策略仍然难以捉摸。尽管细胞外蛋白(包括胶原蛋白、蛋白聚糖和糖蛋白)水平升高与化疗耐药有关,但在药物开发和筛选过程中往往缺乏这些蛋白。细胞外基质(ECM)的生物物理和生化信号决定了细胞表型,并影响肿瘤的进展和治疗反应。然而,许多最先进的肿瘤模型未能模拟肿瘤微环境(TME)的复杂性,并且省略了关键的信号成分。在本文中,我们对两种互穿网络(IPN)水凝胶支架平台进行了表征,这两种平台由藻酸盐-胶原蛋白或琼脂糖-胶原蛋白组成,可作为上皮性卵巢癌 ECM 的 3D 体外模型。这些高度可调、可注塑成型且价格低廉的 IPN 复制了卵巢 TME 中存在的关键控制物理和化学信号。此外,我们还建立了一种有效的细胞友好型活细胞回收方法,以在封装后回收细胞。最后,通过增加 3D 体外 ECM 模型中的支架刚度,证明了卵巢癌中的功能机械转导。有了这些特性,琼脂糖-胶原蛋白和藻酸盐-胶原蛋白水凝胶为上皮性癌症中机械生物学的研究提供了一个强大的 TME。
卵巢癌是当今女性患有的最致命的妇科癌症。在这里,我们提出了 3D 互穿平台的开发、表征和验证,以改变标准体外模型的范式。这些模型有助于阐明生物物理和生化线索在卵巢癌进展中的作用。琼脂糖-胶原蛋白和藻酸盐-胶原蛋白互穿网络(IPN)水凝胶易于制造、价格低廉,并且可以进行修改以创建具有定制机械刚度和生物粘附基序浓度的 IPN 水凝胶。鉴于对生物物理特性在卵巢癌中的作用的研究结果不一致,我们认为 IPN 平台对于揭示分子驱动因素至关重要。我们还期望这些平台能够广泛应用于涉及实体瘤机械生物学的研究。