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PAX基因:在发育、癌症及其他疾病中的作用

The PAX Genes: Roles in Development, Cancer, and Other Diseases.

作者信息

Shaw Taryn, Barr Frederic G, Üren Aykut

机构信息

Department of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC 20001, USA.

Laboratory of Pathology, National Cancer Institute, Bethesda, MD 20892, USA.

出版信息

Cancers (Basel). 2024 Feb 29;16(5):1022. doi: 10.3390/cancers16051022.

Abstract

Since their 1986 discovery in , Paired box (PAX) genes have been shown to play major roles in the early development of the eye, muscle, skeleton, kidney, and other organs. Consistent with their roles as master regulators of tissue formation, the PAX family members are evolutionarily conserved, regulate large transcriptional networks, and in turn can be regulated by a variety of mechanisms. Losses or mutations in these genes can result in developmental disorders or cancers. The precise mechanisms by which PAX genes control disease pathogenesis are well understood in some cases, but much remains to be explored. A deeper understanding of the biology of these genes, therefore, has the potential to aid in the improvement of disease diagnosis and the development of new treatments.

摘要

自1986年在[具体发现地点未给出]被发现以来,配对盒(PAX)基因已被证明在眼睛、肌肉、骨骼、肾脏和其他器官的早期发育中发挥主要作用。与其作为组织形成主要调节因子的作用相一致,PAX家族成员在进化上是保守的,调节大型转录网络,反过来又可通过多种机制进行调节。这些基因的缺失或突变可导致发育障碍或癌症。在某些情况下,人们已经很好地理解了PAX基因控制疾病发病机制的精确机制,但仍有许多有待探索。因此,对这些基因生物学的更深入理解有可能有助于改善疾病诊断和开发新的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5496/10931086/7d3b5246ebc7/cancers-16-01022-g001.jpg

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