AI Article Synopsis

  • Oncogenes, like the Holliday Junction Recognition Protein (HJURP), play a significant role in cancer development, acting as a chaperone for histone H3 and influencing nucleosome composition.
  • HJURP is found on chromosome 2q37.1 and is crucial for assembling centromere structures, with its dysfunction linked to tumorigenesis and poor cancer prognosis.
  • Research indicates that HJURP is often overexpressed in various cancers, promoting cell proliferation and invasiveness, making it a potential target for innovative cancer therapies.

Article Abstract

Oncogenes are increasingly recognized as important factors in the development and progression of cancer. Holliday Junction Recognition Protein (HJURP) is a highly specialized mitogenic protein that is a chaperone protein of histone H3. The HJURP gene is located on chromosome 2q37.1 and is involved in nucleosome composition in the mitotic region, forming a three-dimensional crystal structure with Centromere Protein A (CENP-A) and the histone 4 complex. HJURP is involved in the recruitment and assembly of centromere and kinetochore and plays a key role in stabilizing the chromosome structure of tumor cells, and its dysfunction may contribute to tumorigenesis. In the available studies HJURP is upregulated in a variety of cancer tissues and cancer cell lines and is involved in tumor proliferation, invasion, metastasis and immune response. In an model, overexpression of HJURP in most cancer cell lines promotes cell proliferation and invasiveness, reduces susceptibility to apoptosis, and promotes tumor growth. In addition, upregulation of HJURP was associated with poorer prognosis in a variety of cancers. These properties suggest that HJURP may be a possible target for the treatment of certain cancers. Various studies targeting HJURP as a prognostic and therapeutic target for cancer are gradually attracting interest and attention. This paper reviews the functional and molecular mechanisms of HJURP in a variety of tumor types with the aim of providing new targets for future cancer therapy.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10070699PMC
http://dx.doi.org/10.3389/fcell.2023.1106638DOI Listing

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