{"id":383632,"date":"2023-12-15T10:11:44","date_gmt":"2023-12-15T15:11:44","guid":{"rendered":"https:\/\/platohealth.ai\/wnt-pathway-dysfunction-influences-colorectal-cancer-response-to\/"},"modified":"2023-12-15T10:30:21","modified_gmt":"2023-12-15T15:30:21","slug":"wnt-pathway-dysfunction-influences-colorectal-cancer-response-to","status":"publish","type":"post","link":"https:\/\/platohealth.ai\/wnt-pathway-dysfunction-influences-colorectal-cancer-response-to\/","title":{"rendered":"Wnt pathway dysfunction influences colorectal cancer response to","gt_translate_keys":[{"key":"rendered","format":"text"}]},"content":{"rendered":"

In a rapid communication published in the journal Genes & Diseases<\/em>, has shed light on the role of the Wnt signaling pathway in influencing the immune response of colorectal cancer (CRC) patients. Researchers from Nankai University discovered that abnormalities in this pathway can affect a patient\u2019s response to immunotherapy, paving the way for more tailored treatment strategies. They integrated transcriptome data from 425 CRC patients, aiming to explore the underlying mechanism of MSI. They identified that the Wnt signaling pathway, essential for various cellular processes, showed signs of inhibition in MSI patients. The team also noted a significant down-regulation in mismatch repair enzyme gene MLH1 in these patients. Intriguingly, the expression of the MLH1 gene, crucial for DNA repair, was influenced by the activity of the Wnt signaling pathway. In MSI patients, the canonical Wnt signaling pathway was notably suppressed, resulting in the diminished expression of the mismatch repair enzyme, MLH1. This decrease in MLH1 expression underpins defects in the mismatch repair system, a defining characteristic of MSI. Concurrently, the study identified a down-regulation of SET, another pivotal gene, in these patients. The reduced SET expression correlated with a surge in immune infiltration and activation, hinting at an intensified immune response. Intriguingly, this research posits that MSI patients with such decreased SET expression may exhibit an enhanced responsiveness to immunotherapy, particularly immune checkpoint blockade (ICB).<\/p>\n

The communication indicates that dysfunction in the Wnt signaling pathway could be a driving force behind MSI in CRC. Reduced activity of specific transcription factors led to decreased MLH1 expression, impairing DNA repair mechanisms. Additionally, the role of the SET gene in modulating immune responses provides valuable insights into why MSI patients might respond better to immunotherapy.<\/p>\n

\"Abnormality<\/p>\n

Credit: Genes & Diseases<\/p>\n

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In a rapid communication published in the journal Genes & Diseases<\/em>, has shed light on the role of the Wnt signaling pathway in influencing the immune response of colorectal cancer (CRC) patients. Researchers from Nankai University discovered that abnormalities in this pathway can affect a patient\u2019s response to immunotherapy, paving the way for more tailored treatment strategies. They integrated transcriptome data from 425 CRC patients, aiming to explore the underlying mechanism of MSI. They identified that the Wnt signaling pathway, essential for various cellular processes, showed signs of inhibition in MSI patients. The team also noted a significant down-regulation in mismatch repair enzyme gene MLH1 in these patients. Intriguingly, the expression of the MLH1 gene, crucial for DNA repair, was influenced by the activity of the Wnt signaling pathway. In MSI patients, the canonical Wnt signaling pathway was notably suppressed, resulting in the diminished expression of the mismatch repair enzyme, MLH1. This decrease in MLH1 expression underpins defects in the mismatch repair system, a defining characteristic of MSI. Concurrently, the study identified a down-regulation of SET, another pivotal gene, in these patients. The reduced SET expression correlated with a surge in immune infiltration and activation, hinting at an intensified immune response. Intriguingly, this research posits that MSI patients with such decreased SET expression may exhibit an enhanced responsiveness to immunotherapy, particularly immune checkpoint blockade (ICB).<\/p>\n

The communication indicates that dysfunction in the Wnt signaling pathway could be a driving force behind MSI in CRC. Reduced activity of specific transcription factors led to decreased MLH1 expression, impairing DNA repair mechanisms. Additionally, the role of the SET gene in modulating immune responses provides valuable insights into why MSI patients might respond better to immunotherapy.<\/p>\n

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References<\/p>\n

DOI<\/strong><\/p>\n

10.1016\/j.gendis.2023.03.026<\/p>\n

Original Source URL<\/strong><\/p>\n

https:\/\/doi.org\/10.1016\/j.gendis.2023.03.026<\/p>\n

Funding information<\/strong><\/p>\n

The National Nature Science Foundation of China (81973356, 81902826 and 82273963),
The Natural Science Foundation of Tianjin (21JCZDJC00060 and 21JCYBJC00180),
The Fundamental Research Funds for the Central Universities of Nankai University (ZB22010404, 3206054, 91923101, 63213082, and 92122017).<\/p>\n

About Genes & Diseases<\/em><\/strong><\/p>\n

Genes & Diseases <\/em>is a journal for molecular and translational medicine. The journal primarily focuses on publishing investigations on the molecular bases and experimental therapeutics of human diseases. Publication formats include full length research article, review article, short communication, correspondence, perspectives, commentary, views on news, and research watch.<\/p>\n

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Journal<\/h4>\n

Genes & Diseases<\/p>\n<\/div>\n

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DOI<\/h4>\n

10.1016\/j.gendis.2023.03.026 <\/i><\/p>\n<\/div>\n

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Subject of Research<\/h4>\n

Not applicable<\/p>\n<\/div>\n

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Article Title<\/h4>\n

The dysfunctional Wnt pathway down-regulates MLH1\/SET expression and promotes microsatellite instability and immunotherapy response in colorectal cancer<\/p>\n<\/div>\n

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Article Publication Date<\/h4>\n

30-Aug-2023<\/p>\n<\/div>\n

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COI Statement<\/h4>\n

The authors declare that they have no competing interests<\/p>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n