Department of Cell Pathology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
Department of Neurosurgery, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
Cancer Sci. 2022 Jun;113(6):2129-2143. doi: 10.1111/cas.15349. Epub 2022 Apr 8.
Cholesterol is an essential plasma membrane lipid for the maintenance of cellular homeostasis and cancer cell proliferation. Free cholesterol is harmful to cells; therefore, excessive free cholesterol must be quickly esterified by acetyl-coenzyme A:cholesterol acetyltransferase (ACAT) and exported by scavenger receptor class B member I (SR-BI) or ATP-binding cassette protein A1 from specific cells such as macrophage foam cells, which contain cholesteryl ester-derived vacuoles. Many vacuoles are present in the cytoplasm of Burkitt lymphoma cells. In this study, we observed that these vacuoles are often seen in high-grade lymphomas. Cell culture study using lymphoma cell lines found that esterified cholesterol is the main component of these vacuoles and the expression of cholesterol metabolism-related molecules was significantly upregulated in lymphoma cell lines, with SR-BI and ACAT inhibitors (BLT-1 and CI-976, respectively) impeding lymphoma cell proliferation. Cytoplasmic free cholesterol was increased by ACAT and SR-BI inhibitors, and the accumulation of free cholesterol induced lymphoma cell apoptosis by inducing endoplasmic reticulum stress. Furthermore, synergistic effects of SR-BI and ACAT inhibitors were observed in a preclinical study. Treatment with SR-BI inhibitor suppressed lymphoma progression in a tumor-bearing mouse model, whereas ACAT inhibitor did not. Therefore, SR-BI inhibitors are potential new antilymphoma therapeutics that target cholesterol metabolism.
胆固醇是维持细胞内环境稳定和癌细胞增殖的必需的质膜脂质。游离胆固醇对细胞有害;因此,过量的游离胆固醇必须迅速被乙酰辅酶 A:胆固醇乙酰转移酶(ACAT)酯化,并通过清道夫受体 B 类成员 I(SR-BI)或 ATP 结合盒蛋白 A1 从特定细胞(如巨噬细胞泡沫细胞)中输出,这些细胞含有胆固醇酯衍生的空泡。许多空泡存在于伯基特淋巴瘤细胞的细胞质中。在这项研究中,我们观察到这些空泡在高级别淋巴瘤中经常出现。使用淋巴瘤细胞系进行的细胞培养研究发现,酯化胆固醇是这些空泡的主要成分,并且胆固醇代谢相关分子的表达在淋巴瘤细胞系中显著上调,SR-BI 和 ACAT 抑制剂(分别为 BLT-1 和 CI-976)阻碍淋巴瘤细胞增殖。ACAT 和 SR-BI 抑制剂增加细胞质游离胆固醇,游离胆固醇的积累通过诱导内质网应激诱导淋巴瘤细胞凋亡。此外,在临床前研究中观察到了 SR-BI 和 ACAT 抑制剂的协同作用。用 SR-BI 抑制剂治疗可抑制荷瘤小鼠模型中的淋巴瘤进展,而 ACAT 抑制剂则不能。因此,SR-BI 抑制剂是针对胆固醇代谢的潜在新型抗淋巴瘤治疗药物。