Cell Biology and Molecular Genetics Division, Yenepoya Research Centre, Yenepoya (Deemed to be) University, 3rd Floor, Academic Block, University Road, Deralakatte, Mangalore, Karnataka, 575018, India.
Cell Oncol (Dordr). 2024 Oct;47(5):1607-1626. doi: 10.1007/s13402-024-00988-w. Epub 2024 Sep 16.
The c-MPL-TPO axis regulates hematopoiesis by activating various signalling cascades, including JAK/STAT, MAPK/ERK, and PIK3/AKT. Here, we have summarized how TPO is regulated by c-MPL and, how mutations in the c-MPL regulate hematopoiesis. We also focus on its non-hematological regulatory role in diseases like Unstable Angina and pathways like DNA damage repair, skeletal homeostasis, & apoptotic regulation of neurons/HSCs at the embryonic state. We discuss the therapeutic efficiency of c-MPL and, its potential to be developed as a bio-marker for detecting metastasis and development of chemo-resistance in various cancers, justifying the multifaceted nature of c-MPL. We have also highlighted the importance of c-MPL isoforms and their stoichiometry in controlling the HSC quiescent and proliferative state. The regulation of the ratio of different isoforms through gene-therapy can open future therapeutic avenues. A systematic understanding of c-MPL-isoforms would undoubtedly take one step closer to facilitating c-MPL from basic-research towards translational medicine.
c-MPL-TPO 轴通过激活各种信号级联来调节造血,包括 JAK/STAT、MAPK/ERK 和 PIK3/AKT。在这里,我们总结了 TPO 如何受 c-MPL 调节,以及 c-MPL 中的突变如何调节造血。我们还重点关注了它在不稳定型心绞痛等疾病中的非造血调节作用,以及在 DNA 损伤修复、骨骼稳态和胚胎状态下神经元/HSCs 的凋亡调节等途径中的作用。我们讨论了 c-MPL 的治疗效果及其作为检测各种癌症转移和化疗耐药性发展的生物标志物的潜力,证明了 c-MPL 的多面性。我们还强调了 c-MPL 同工型及其在控制 HSC 静止和增殖状态中的比例的重要性。通过基因治疗调节不同同工型的比例可以为未来的治疗方法开辟新途径。对 c-MPL 同工型的系统理解无疑将有助于将 c-MPL 从基础研究推向转化医学。