piRNA in Machine-Learning-Based Diagnostics of Colorectal Cancer

被引:0
作者
Li, Sienna [1 ]
Kouznetsova, Valentina L. [1 ,2 ]
Kesari, Santosh [3 ]
Tsigelny, Igor F. [1 ,2 ,4 ]
机构
[1] CureSci Inst, San Diego, CA 92121 USA
[2] Univ Calif San Diego, San Diego Supercomp Ctr, La Jolla, CA 92093 USA
[3] Pacific Neurosci Inst, Santa Monica, CA 90404 USA
[4] Univ Calif San Diego, Dept Neurosci, La Jolla, CA 92093 USA
来源
MOLECULES | 2024年 / 29卷 / 18期
关键词
piRNA; machine learning; colorectal cancer; diagnostics;
D O I
10.3390/molecules29184311
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Objective biomarkers are crucial for early diagnosis to promote treatment and raise survival rates for diseases. With the smallest non-coding RNAs-piwi-RNAs (piRNAs)-and their transcripts, we sought to identify if these piRNAs could be used as biomarkers for colorectal cancer (CRC). Using previously published data from serum samples of patients with CRC, 13 differently expressed piRNAs were selected as potential biomarkers. With this data, we developed a machine learning (ML) algorithm and created 1020 different piRNA sequence descriptors. With the Na & iuml;ve Bayes Multinomial classifier, we were able to isolate the 27 most influential sequence descriptors and achieve an accuracy of 96.4%. To test the validity of our model, we used data from piRBase with known associations with CRC that we did not use to train the ML model. We were able to achieve an accuracy of 85.7% with these new independent data. To further validate our model, we also tested data from unrelated diseases, including piRNAs with a correlation to breast cancer and no proven correlation to CRC. The model scored 44.4% on these piRNAs, showing that it can identify a difference between biomarkers of CRC and biomarkers of other diseases. The final results show that our model is an effective tool for diagnosing colorectal cancer. We believe that in the future, this model will prove useful for colorectal cancer and other diseases diagnostics.
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页数:10
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