AI Article Synopsis

  • Inhibition of WEE1, which controls a checkpoint in the cell cycle, triggers cell death by forcing cell division without fixing DNA damage, but its impact on colorectal cancer (CRC) immunity wasn't well understood.
  • Researchers found that WEE1 expression was not linked to CRC characteristics but that WEE1 inhibitors reduced cancer cell growth and increased cell death, particularly in mutated cells.
  • In mouse models, WEE1 inhibitor treatment resulted in smaller tumors and enhanced immune responses against the cancer, indicating its potential benefits for CRC patients, especially those with specific mutations.

Article Abstract

Inhibition of WEE1, a key regulator of the G2/M checkpoint of the cell cycle, induces apoptosis by initiating mitosis without repairing DNA damage. However, the effects of WEE1 inhibitors on the tumor immune microenvironment in colorectal cancer (CRC) remain unclear. Here, we investigated the association between WEE1 expression and CRC clinicopathological features using surgically resected CRC specimens and assessed the antitumor effects of a WEE1 inhibitor using CRC cell lines and orthotopic transplantation mouse models. WEE1 expression was not correlated with the clinicopathological features of CRC. The WEE1 inhibitor suppressed cell proliferation in a concentration-dependent manner in all CRC cell lines. It also increased the percentage of cells in the G2/M phase and apoptotic cells, especially in cell lines with mutations, but did not alter these cell percentages in most wild-type cell lines. In the orthotopic mouse model of CRC, tumor volume was significantly reduced in the WEE1 inhibitor-treated group compared to that in the control group. RNA sequencing and immunohistochemistry analyses of mouse tumors revealed that treatment with the WEE1 inhibitor activated tumor immunity and suppressed stromal reactions. These results demonstrate the potential antitumor effects of WEE1 inhibitors in CRC, particularly in patients with mutations.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11429655PMC
http://dx.doi.org/10.3390/cancers16183136DOI Listing

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