4.7 Article

Co-inhibition of Aurora A and Haspin kinases enhances survivin blockage and p53 induction for mitotic catastrophe and apoptosis in human colorectal cancer

Journal

BIOCHEMICAL PHARMACOLOGY
Volume 206, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bcp.2022.115289

Keywords

Colorectal cancer; Aurora A; Haspin; Survivin; p53

Funding

  1. Ministry of Science and Technology in Taiwan [MOST 106-2320-B-009-001-MY3, MOST109-2320-B-009-003-MY3, MOST109-2320-B-009-004-MY3]
  2. Center For Intelligent Drug Systems and Smart Biodevices (IDS2B)
  3. Ministry of Education (MOE) in Taiwan
  4. NCTU-KMU joint research project [NCTU-KMU-109-IF-01]
  5. Confocal Microscope System (MCMS)

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In colorectal cancer patients, the levels of Haspin and phospho-H3T3 protein are highly expressed. Overexpression of Haspin increases the levels of p-H3T3 and survivin proteins in CRC cells. Knockdown of Aurora A gene leads to abnormal chromosome segregation, mitotic catastrophe and cell growth inhibition. Combined treatment of Aurora A and Haspin inhibitors enhances apoptosis and tumor inhibition in CRC.
Colorectal cancer (CRC) is a leading cause and mortality worldwide. Aurora A and haspin kinases act pivotal roles in mitotic progression. However, the blockage of Aurora A and Haspin for CRC therapy is still unclear. Here we show that the Haspin and p-H3T3 protein levels were highly expressed in CRC tumor tissues of clinical pa-tients. Overexpression of Haspin increased the protein levels of p-H3T3 and survivin in human CRC cells; conversely, the protein levels of p-H3T3 and survivin were decreased by the Haspin gene knockdown. Moreover, the gene knockdown of Aurora A induced abnormal chromosome segregation, mitotic catastrophe, and cell growth inhibition. Combined targeted by co-treatment of CHR6494, a Haspin inhibitor, and MLN8237, an Aurora A inhibitor, enhanced apoptosis and CRC tumor inhibition. MLN8237 and CHR6494 induced abnormal chro-mosome segregation and mitotic catastrophe. Meanwhile, MLN8237 and CHR6494 inhibited survivin protein levels but conversely induced p53 protein expression. Ectopic survivin expression by transfection with a survivin-expressed vector resisted the cell death in the MLN8237-and CHR6494-treated cells. In contrast, the existence of functional p53 increased the apoptotic levels by treatment with MLN8237 and CHR6494. Co-treatment of CHR6494 and MLN8237 enhanced the blockage of human CRC xenograft tumors in nude mice. Taken together, co-inhibition of Aurora A and Haspin enhances survivin inhibition, p53 pathway induction, mitotic catastrophe, apoptosis and tumor inhibition that may provide a potential strategy for CRC therapy.

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