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Information about immune cell proportions and tumor stage improves the prediction of recurrence in patients with colorectal cancer

Predicting cancer recurrence is essential to improving the clinical outcomes of patients with colorectal cancer (CRC). Although tumor stage information has been used as a guideline to predict CRC recurrence, patients with the same stage show different clinical outcomes. Therefore, there is a need to...

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Detalles Bibliográficos
Autores principales: Kong, JungHo, Kim, Jinho, Kim, Donghyo, Lee, Kwanghwan, Lee, Juhun, Han, Seong Kyu, Kim, Inhae, Lim, Seongsu, Park, Minhyuk, Shin, Seungho, Lee, Woo Yong, Yun, Seong Hyeon, Kim, Hee Cheol, Hong, Hye Kyung, Cho, Yong Beom, Park, Donghyun, Kim, Sanguk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10318368/
https://www.ncbi.nlm.nih.gov/pubmed/37409049
http://dx.doi.org/10.1016/j.patter.2023.100736
Descripción
Sumario:Predicting cancer recurrence is essential to improving the clinical outcomes of patients with colorectal cancer (CRC). Although tumor stage information has been used as a guideline to predict CRC recurrence, patients with the same stage show different clinical outcomes. Therefore, there is a need to develop a method to identify additional features for CRC recurrence prediction. Here, we developed a network-integrated multiomics (NIMO) approach to select appropriate transcriptome signatures for better CRC recurrence prediction by comparing the methylation signatures of immune cells. We validated the performance of the CRC recurrence prediction based on two independent retrospective cohorts of 114 and 110 patients. Moreover, to confirm that the prediction was improved, we used both NIMO-based immune cell proportions and TNM (tumor, node, metastasis) stage data. This work demonstrates the importance of (1) using both immune cell composition and TNM stage data and (2) identifying robust immune cell marker genes to improve CRC recurrence prediction.