巨噬细胞移动抑制因子
持久性(不连续性)
慢性淋巴细胞白血病
梅克尔细胞癌
白血病抑制因子
癌症研究
白血病
巨噬细胞
免疫学
抑制性突触后电位
生物
医学
癌
内科学
细胞因子
白细胞介素6
遗传学
体外
岩土工程
工程类
作者
Gabriel F. Alencar,Haroldo J. Rodriguez,Thomas H. Pulliam,Allison J. Remington,Macy W. Gilmour,Rian Alam,Austin J. Jabbour,Logan J. Mullen,Blair L. DeBuysscher,Paul Nghiem,Justin J. Taylor
标识
DOI:10.1101/2024.09.09.611517
摘要
Abstract While concurrent diagnoses of Merkel cell carcinoma (MCC) and other cancers, like Chronic lymphocytic leukemia (CLL), are rare, patients with MCC have a 30-fold higher incidence of CLL. While these increases have been attributed to the ability of CLL to suppress immune responses allowing for the emergence of MCC, here we found evidence that MCC could support the persistence of CLL. Using single cell sequencing approaches and computational analyses of MCC and CLL from a patient where both cancers were present in the same lymph node, we found that production of macrophage migration inhibitory factor (MIF) by MCC could promote the persistence of CLL through stimulation of CD74 and CXCR4. These results may explain why blood cell counts rapidly normalized after treatment for MCC and were maintained at normal levels despite the absence of treatment for CLL. Abstract Figure
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