Arundhathi J R Dev, Mathur Sandeep R, Gogia Ajay, Deo S V S, Mohapatra Purusottam, Prasad Chandra Prakash
Department of Medical Oncology, Dr BRA IRCH, AIIMS, New Delhi, 110029, India.
Department of Pathology, Dr BRA IRCH, AIIMS, New Delhi, 110029, India.
Mol Biol Rep. 2021 May;48(5):4733-4745. doi: 10.1007/s11033-021-06414-w. Epub 2021 May 28.
Among breast cancer subtypes, the triple negative breast cancer (TNBC) has the worst prognosis. In absence of any permitted targeted therapy, standard chemotherapy is the mainstay for TNBC treatment. Hence, there is a crucial need to identify potential druggable targets in TNBCs for its effective treatment. In recent times, metabolic reprogramming has emerged as cancer cells hallmark, wherein cancer cells display discrete metabolic phenotypes to fuel cell progression and metastasis. Altered glycolysis is one such phenotype, in which even in oxygen abundance majority of cancer cells harvest considerable amount of energy through elevated glycolytic-flux. In the present review, we attempt to summarize the role of key glycolytic enzymes i.e. HK, Hexokinase; PFK, Phosphofructokinase; PKM2, Pyruvate kinase isozyme type 2; and LDH, Lactate dehydrogenase in TNBCs, and possible therapeutic options presently available.
在乳腺癌亚型中,三阴性乳腺癌(TNBC)的预后最差。由于缺乏任何许可的靶向治疗方法,标准化化疗是TNBC治疗的主要手段。因此,迫切需要在TNBC中确定潜在的可药物化靶点以实现其有效治疗。近年来,代谢重编程已成为癌细胞的标志,其中癌细胞表现出离散的代谢表型以促进细胞进展和转移。糖酵解改变就是这样一种表型,即使在氧气充足的情况下,大多数癌细胞也通过升高的糖酵解通量获取大量能量。在本综述中,我们试图总结关键糖酵解酶,即己糖激酶(HK)、磷酸果糖激酶(PFK)、丙酮酸激酶同工酶2型(PKM2)和乳酸脱氢酶(LDH)在TNBC中的作用,以及目前可用的可能治疗选择。