Differential levels of circulating RNAs prior to endometrial cancer diagnosis
Endometrial cancer (EC) is one of the most common female cancers and there is currently no routine screening strategy for early detection. An altered abundance of circulating microRNAs (miRNAs) and other RNA classes have the potential as early cancer biomarkers. We analyzed circulating RNA levels us...
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Published in | International journal of cancer Vol. 155; no. 5; pp. 946 - 956 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
Wiley Subscription Services, Inc
01.09.2024
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Online Access | Get full text |
ISSN | 0020-7136 1097-0215 1097-0215 |
DOI | 10.1002/ijc.34951 |
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Abstract | Endometrial cancer (EC) is one of the most common female cancers and there is currently no routine screening strategy for early detection. An altered abundance of circulating microRNAs (miRNAs) and other RNA classes have the potential as early cancer biomarkers. We analyzed circulating RNA levels using small RNA sequencing, targeting RNAs in the size range of 17–47 nucleotides, in EC patients with samples collected prior to diagnosis compared to cancer‐free controls. The analysis included 316 cases with samples collected 1–11 years prior to EC diagnosis, and 316 matched controls, both from the Janus Serum Bank cohort in Norway. We identified differentially abundant (DA) miRNAs, isomiRs, and small nuclear RNAs between EC cases and controls. The top EC DA miRNAs were miR‐155‐5p, miR‐200b‐3p, miR‐589‐5p, miR‐151a‐5p, miR‐543, miR‐485‐5p, miR‐625‐p, and miR‐671‐3p. miR‐200b‐3p was previously reported to be among one of the top miRNAs with higher abundance in EC cases. We observed 47, 41, and 32 DA miRNAs for EC interacting with BMI, smoking status, and physical activity, respectively, including two miRNAs (miR‐223‐3p and miR‐29b‐3p) interacting with all three factors. The circulating RNAs are altered and show temporal dynamics prior to EC diagnosis. Notably, DA miRNAs for EC had the lowest
q
‐value 4.39–6.66 years before diagnosis. Enrichment analysis of miRNAs showed that signaling pathways Fc epsilon RI, prolactin, toll‐like receptor, and VEGF had the strongest associations. |
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AbstractList | Endometrial cancer (EC) is one of the most common female cancers and there is currently no routine screening strategy for early detection. An altered abundance of circulating microRNAs (miRNAs) and other RNA classes have the potential as early cancer biomarkers. We analyzed circulating RNA levels using small RNA sequencing, targeting RNAs in the size range of 17–47 nucleotides, in EC patients with samples collected prior to diagnosis compared to cancer‐free controls. The analysis included 316 cases with samples collected 1–11 years prior to EC diagnosis, and 316 matched controls, both from the Janus Serum Bank cohort in Norway. We identified differentially abundant (DA) miRNAs, isomiRs, and small nuclear RNAs between EC cases and controls. The top EC DA miRNAs were miR‐155‐5p, miR‐200b‐3p, miR‐589‐5p, miR‐151a‐5p, miR‐543, miR‐485‐5p, miR‐625‐p, and miR‐671‐3p. miR‐200b‐3p was previously reported to be among one of the top miRNAs with higher abundance in EC cases. We observed 47, 41, and 32 DA miRNAs for EC interacting with BMI, smoking status, and physical activity, respectively, including two miRNAs (miR‐223‐3p and miR‐29b‐3p) interacting with all three factors. The circulating RNAs are altered and show temporal dynamics prior to EC diagnosis. Notably, DA miRNAs for EC had the lowest q‐value 4.39–6.66 years before diagnosis. Enrichment analysis of miRNAs showed that signaling pathways Fc epsilon RI, prolactin, toll‐like receptor, and VEGF had the strongest associations. Endometrial cancer (EC) is one of the most common female cancers and there is currently no routine screening strategy for early detection. An altered abundance of circulating microRNAs (miRNAs) and other RNA classes have the potential as early cancer biomarkers. We analyzed circulating RNA levels using small RNA sequencing, targeting RNAs in the size range of 17–47 nucleotides, in EC patients with samples collected prior to diagnosis compared to cancer‐free controls. The analysis included 316 cases with samples collected 1–11 years prior to EC diagnosis, and 316 matched controls, both from the Janus Serum Bank cohort in Norway. We identified differentially abundant (DA) miRNAs, isomiRs, and small nuclear RNAs between EC cases and controls. The top EC DA miRNAs were miR‐155‐5p, miR‐200b‐3p, miR‐589‐5p, miR‐151a‐5p, miR‐543, miR‐485‐5p, miR‐625‐p, and miR‐671‐3p. miR‐200b‐3p was previously reported to be among one of the top miRNAs with higher abundance in EC cases. We observed 47, 41, and 32 DA miRNAs for EC interacting with BMI, smoking status, and physical activity, respectively, including two miRNAs (miR‐223‐3p and miR‐29b‐3p) interacting with all three factors. The circulating RNAs are altered and show temporal dynamics prior to EC diagnosis. Notably, DA miRNAs for EC had the lowest q ‐value 4.39–6.66 years before diagnosis. Enrichment analysis of miRNAs showed that signaling pathways Fc epsilon RI, prolactin, toll‐like receptor, and VEGF had the strongest associations. Endometrial cancer (EC) is one of the most common female cancers and there is currently no routine screening strategy for early detection. An altered abundance of circulating microRNAs (miRNAs) and other RNA classes have the potential as early cancer biomarkers. We analyzed circulating RNA levels using small RNA sequencing, targeting RNAs in the size range of 17-47 nucleotides, in EC patients with samples collected prior to diagnosis compared to cancer-free controls. The analysis included 316 cases with samples collected 1-11 years prior to EC diagnosis, and 316 matched controls, both from the Janus Serum Bank cohort in Norway. We identified differentially abundant (DA) miRNAs, isomiRs, and small nuclear RNAs between EC cases and controls. The top EC DA miRNAs were miR-155-5p, miR-200b-3p, miR-589-5p, miR-151a-5p, miR-543, miR-485-5p, miR-625-p, and miR-671-3p. miR-200b-3p was previously reported to be among one of the top miRNAs with higher abundance in EC cases. We observed 47, 41, and 32 DA miRNAs for EC interacting with BMI, smoking status, and physical activity, respectively, including two miRNAs (miR-223-3p and miR-29b-3p) interacting with all three factors. The circulating RNAs are altered and show temporal dynamics prior to EC diagnosis. Notably, DA miRNAs for EC had the lowest q-value 4.39-6.66 years before diagnosis. Enrichment analysis of miRNAs showed that signaling pathways Fc epsilon RI, prolactin, toll-like receptor, and VEGF had the strongest associations.Endometrial cancer (EC) is one of the most common female cancers and there is currently no routine screening strategy for early detection. An altered abundance of circulating microRNAs (miRNAs) and other RNA classes have the potential as early cancer biomarkers. We analyzed circulating RNA levels using small RNA sequencing, targeting RNAs in the size range of 17-47 nucleotides, in EC patients with samples collected prior to diagnosis compared to cancer-free controls. The analysis included 316 cases with samples collected 1-11 years prior to EC diagnosis, and 316 matched controls, both from the Janus Serum Bank cohort in Norway. We identified differentially abundant (DA) miRNAs, isomiRs, and small nuclear RNAs between EC cases and controls. The top EC DA miRNAs were miR-155-5p, miR-200b-3p, miR-589-5p, miR-151a-5p, miR-543, miR-485-5p, miR-625-p, and miR-671-3p. miR-200b-3p was previously reported to be among one of the top miRNAs with higher abundance in EC cases. We observed 47, 41, and 32 DA miRNAs for EC interacting with BMI, smoking status, and physical activity, respectively, including two miRNAs (miR-223-3p and miR-29b-3p) interacting with all three factors. The circulating RNAs are altered and show temporal dynamics prior to EC diagnosis. Notably, DA miRNAs for EC had the lowest q-value 4.39-6.66 years before diagnosis. Enrichment analysis of miRNAs showed that signaling pathways Fc epsilon RI, prolactin, toll-like receptor, and VEGF had the strongest associations. |
Author | Rostami, Sina Fortner, Renée Turzanski Pestarino, Luca Haaland, Øystein Ariansen Wiklund, Fredrik Lie, Rolv T. Bjørge, Tone Rounge, Trine B. Langseth, Hilde Lyle, Robert |
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Cites_doi | 10.1042/BSR20210111 10.1080/15476286.2017.1403003 10.1016/j.ejca.2008.10.037 10.1158/1055‐9965 10.1111/j.1600‐0463.2008.00015.x 10.3390/cells11111836 10.1136/jmedgenet‐2021‐108327 10.7554/eLife.28932 10.3892/or.2022.8307 10.1186/s13104‐016‐1900‐2 10.1016/j.soncn.2019.02.002 10.1038/s41598‐018‐35974‐4 10.2147/OTT.S193097 10.1089/cbr.2018.2766 10.1016/j.bpobgyn.2019.12.006 10.1056/NEJMsr1606602 10.7554/eLife.71035 10.1038/s41587‐020‐0439‐x 10.1146/annurev‐genet‐120213‐092023 10.7717/peerj.4262 10.1093/ije/dyw302 10.1038/nmeth.1923 10.3322/caac.21660 10.1007/s00404‐014‐3219‐3 10.3390/ijms17050709 10.3389/fonc.2020.01415 10.1093/cvr/cvr097 10.1186/s13148‐018‐0492‐1 10.1186/s12943‐021‐01352‐4 10.1093/nar/gkv007 10.1093/nar/gky1141 10.1038/bjc.2015.253 10.1111/jcmm.15111 10.1093/nar/gkaa467 10.1093/bioinformatics/btp616 10.1016/S0140‐6736(22)00323‐3 10.1186/s41544‐019‐0039‐4 10.3389/fendo.2018.00402 10.1038/ncomms12436 10.3892/or.2011.1372 10.1093/nar/gkaa309 10.1177/0300060519834815 10.1007/s00432‐015‐2095‐y 10.3390/biology8010001 10.1093/ije/dyw027 10.1093/nar/gkz896 10.18632/oncotarget.4738 |
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Keywords | cell‐free nucleic acids RNA RNA‐sequencing endometrial neoplasms |
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References | e_1_2_11_32_1 e_1_2_11_30_1 e_1_2_11_36_1 e_1_2_11_51_1 e_1_2_11_13_1 e_1_2_11_34_1 e_1_2_11_11_1 e_1_2_11_29_1 e_1_2_11_6_1 e_1_2_11_27_1 e_1_2_11_4_1 e_1_2_11_48_1 e_1_2_11_2_1 e_1_2_11_20_1 e_1_2_11_45_1 e_1_2_11_47_1 e_1_2_11_24_1 e_1_2_11_41_1 e_1_2_11_8_1 e_1_2_11_22_1 e_1_2_11_43_1 e_1_2_11_17_1 e_1_2_11_15_1 e_1_2_11_38_1 e_1_2_11_19_1 e_1_2_11_50_1 e_1_2_11_10_1 e_1_2_11_31_1 e_1_2_11_14_1 e_1_2_11_35_1 e_1_2_11_12_1 e_1_2_11_33_1 e_1_2_11_7_1 e_1_2_11_28_1 e_1_2_11_5_1 e_1_2_11_26_1 e_1_2_11_3_1 e_1_2_11_49_1 e_1_2_11_21_1 e_1_2_11_44_1 e_1_2_11_46_1 e_1_2_11_25_1 e_1_2_11_40_1 e_1_2_11_9_1 e_1_2_11_23_1 e_1_2_11_42_1 e_1_2_11_18_1 e_1_2_11_16_1 e_1_2_11_37_1 e_1_2_11_39_1 |
References_xml | – ident: e_1_2_11_16_1 doi: 10.1042/BSR20210111 – ident: e_1_2_11_22_1 doi: 10.1080/15476286.2017.1403003 – ident: e_1_2_11_19_1 doi: 10.1016/j.ejca.2008.10.037 – ident: e_1_2_11_28_1 doi: 10.1158/1055‐9965 – ident: e_1_2_11_48_1 doi: 10.1111/j.1600‐0463.2008.00015.x – ident: e_1_2_11_15_1 doi: 10.3390/cells11111836 – ident: e_1_2_11_8_1 doi: 10.1136/jmedgenet‐2021‐108327 – ident: e_1_2_11_36_1 doi: 10.7554/eLife.28932 – ident: e_1_2_11_41_1 doi: 10.3892/or.2022.8307 – ident: e_1_2_11_23_1 doi: 10.1186/s13104‐016‐1900‐2 – ident: e_1_2_11_6_1 doi: 10.1016/j.soncn.2019.02.002 – ident: e_1_2_11_31_1 doi: 10.1038/s41598‐018‐35974‐4 – ident: e_1_2_11_38_1 doi: 10.2147/OTT.S193097 – ident: e_1_2_11_43_1 doi: 10.1089/cbr.2018.2766 – ident: e_1_2_11_7_1 doi: 10.1016/j.bpobgyn.2019.12.006 – ident: e_1_2_11_5_1 doi: 10.1056/NEJMsr1606602 – ident: e_1_2_11_11_1 doi: 10.7554/eLife.71035 – ident: e_1_2_11_25_1 doi: 10.1038/s41587‐020‐0439‐x – ident: e_1_2_11_27_1 doi: 10.1146/annurev‐genet‐120213‐092023 – ident: e_1_2_11_33_1 doi: 10.7717/peerj.4262 – ident: e_1_2_11_20_1 doi: 10.1093/ije/dyw302 – ident: e_1_2_11_24_1 doi: 10.1038/nmeth.1923 – ident: e_1_2_11_3_1 doi: 10.3322/caac.21660 – ident: e_1_2_11_44_1 doi: 10.1007/s00404‐014‐3219‐3 – ident: e_1_2_11_40_1 doi: 10.3390/ijms17050709 – ident: e_1_2_11_37_1 doi: 10.3389/fonc.2020.01415 – ident: e_1_2_11_12_1 doi: 10.1093/cvr/cvr097 – ident: e_1_2_11_10_1 doi: 10.1186/s13148‐018‐0492‐1 – ident: e_1_2_11_17_1 doi: 10.1186/s12943‐021‐01352‐4 – ident: e_1_2_11_30_1 doi: 10.1093/nar/gkv007 – ident: e_1_2_11_2_1 – ident: e_1_2_11_21_1 – ident: e_1_2_11_26_1 doi: 10.1093/nar/gky1141 – ident: e_1_2_11_14_1 doi: 10.1038/bjc.2015.253 – ident: e_1_2_11_42_1 doi: 10.1111/jcmm.15111 – ident: e_1_2_11_34_1 doi: 10.1093/nar/gkaa467 – ident: e_1_2_11_29_1 doi: 10.1093/bioinformatics/btp616 – ident: e_1_2_11_51_1 – ident: e_1_2_11_4_1 doi: 10.1016/S0140‐6736(22)00323‐3 – ident: e_1_2_11_9_1 doi: 10.1186/s41544‐019‐0039‐4 – ident: e_1_2_11_13_1 doi: 10.3389/fendo.2018.00402 – ident: e_1_2_11_46_1 doi: 10.1038/ncomms12436 – ident: e_1_2_11_39_1 doi: 10.3892/or.2011.1372 – ident: e_1_2_11_32_1 doi: 10.1093/nar/gkaa309 – ident: e_1_2_11_47_1 doi: 10.1177/0300060519834815 – ident: e_1_2_11_49_1 doi: 10.1007/s00432‐015‐2095‐y – ident: e_1_2_11_50_1 doi: 10.3390/biology8010001 – ident: e_1_2_11_18_1 doi: 10.1093/ije/dyw027 – ident: e_1_2_11_35_1 doi: 10.1093/nar/gkz896 – ident: e_1_2_11_45_1 doi: 10.18632/oncotarget.4738 |
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Snippet | Endometrial cancer (EC) is one of the most common female cancers and there is currently no routine screening strategy for early detection. An altered abundance... |
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SubjectTerms | Adult Aged Biomarkers, Tumor - blood Biomarkers, Tumor - genetics Case-Control Studies Circulating MicroRNA - blood Diagnosis Endometrial cancer Endometrial Neoplasms - blood Endometrial Neoplasms - diagnosis Endometrial Neoplasms - genetics Endometrium Exercise Fc receptors Female Gene Expression Regulation, Neoplastic Humans Medical diagnosis MicroRNAs MicroRNAs - blood MicroRNAs - genetics Middle Aged miRNA Norway - epidemiology Nucleotides Physical activity Prolactin Ribonucleic acid RNA Smoking Uterine cancer Vascular endothelial growth factor Womens health |
Title | Differential levels of circulating RNAs prior to endometrial cancer diagnosis |
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