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Effect of genetic variation in Notch regulator DTX1 on SCLC prognosis compared with the effect on NSCLC prongosis
Deltex‐1 (DTX1) is a negative regulator of the Notch signaling pathway. Here, we investigated the clinical effect of DTX1 rs1732786A > G, which is associated with better prognosis in patients with early‐stage non‐small cell lung cancer (NSCLC), in 261 patients with small cell lung cancer (SCLC)....
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Australia, Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7471053/ https://www.ncbi.nlm.nih.gov/pubmed/32700476 http://dx.doi.org/10.1111/1759-7714.13566 |
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author | Yoo, Seung Soo Lee, Jang Hyuck Hong, Mi Jeong Choi, Jin Eun Kang, Hyo‐Gyoung Do, Sook Kyung Kim, Ji Hyun Baek, Sun Ah Choi, Sun Ha Lee, Won Kee Lee, Yong Hoon Seo, Hyewon Lee, Jaehee Lee, Shin Yup Cha, Seung Ick Kim, Chang Ho Park, Jae Yong |
author_facet | Yoo, Seung Soo Lee, Jang Hyuck Hong, Mi Jeong Choi, Jin Eun Kang, Hyo‐Gyoung Do, Sook Kyung Kim, Ji Hyun Baek, Sun Ah Choi, Sun Ha Lee, Won Kee Lee, Yong Hoon Seo, Hyewon Lee, Jaehee Lee, Shin Yup Cha, Seung Ick Kim, Chang Ho Park, Jae Yong |
author_sort | Yoo, Seung Soo |
collection | PubMed |
description | Deltex‐1 (DTX1) is a negative regulator of the Notch signaling pathway. Here, we investigated the clinical effect of DTX1 rs1732786A > G, which is associated with better prognosis in patients with early‐stage non‐small cell lung cancer (NSCLC), in 261 patients with small cell lung cancer (SCLC). DTX1 rs1732786A > G was associated with a significantly worse chemotherapy response and lower overall survival in the codominant model (odds ratio = 0.42, 95% confidence interval [CI]: 0.26–0.66, P = 2 × 10(−4); hazard ratio = 1.47, 95% CI: 1.17–1.84, P = 0.001, respectively). An in vitro luciferase assay was performed, and the 1732786G allele demonstrated significantly higher promoter activity than the 1732786A allele (P = 2 × 10(−7)). In summary, DTX1 rs1732786A > G was associated with poor prognosis in patients with SCLC as opposed to patients with NSCLC. KEY POINTS: SIGNIFICANT FINDINGS OF THE STUDY: DTX1 rs1732786A > G was associated with better prognosis in patients with early‐stage non‐small cell lung cancer (NSCLC) in our previous study. WHAT THIS STUDY ADDS: DTX1 rs1732786A > G was associated with a significantly worse chemotherapy response and lower overall survival in small cell lung cancer (SCLC). |
format | Online Article Text |
id | pubmed-7471053 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley & Sons Australia, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-74710532020-09-11 Effect of genetic variation in Notch regulator DTX1 on SCLC prognosis compared with the effect on NSCLC prongosis Yoo, Seung Soo Lee, Jang Hyuck Hong, Mi Jeong Choi, Jin Eun Kang, Hyo‐Gyoung Do, Sook Kyung Kim, Ji Hyun Baek, Sun Ah Choi, Sun Ha Lee, Won Kee Lee, Yong Hoon Seo, Hyewon Lee, Jaehee Lee, Shin Yup Cha, Seung Ick Kim, Chang Ho Park, Jae Yong Thorac Cancer Brief Reports Deltex‐1 (DTX1) is a negative regulator of the Notch signaling pathway. Here, we investigated the clinical effect of DTX1 rs1732786A > G, which is associated with better prognosis in patients with early‐stage non‐small cell lung cancer (NSCLC), in 261 patients with small cell lung cancer (SCLC). DTX1 rs1732786A > G was associated with a significantly worse chemotherapy response and lower overall survival in the codominant model (odds ratio = 0.42, 95% confidence interval [CI]: 0.26–0.66, P = 2 × 10(−4); hazard ratio = 1.47, 95% CI: 1.17–1.84, P = 0.001, respectively). An in vitro luciferase assay was performed, and the 1732786G allele demonstrated significantly higher promoter activity than the 1732786A allele (P = 2 × 10(−7)). In summary, DTX1 rs1732786A > G was associated with poor prognosis in patients with SCLC as opposed to patients with NSCLC. KEY POINTS: SIGNIFICANT FINDINGS OF THE STUDY: DTX1 rs1732786A > G was associated with better prognosis in patients with early‐stage non‐small cell lung cancer (NSCLC) in our previous study. WHAT THIS STUDY ADDS: DTX1 rs1732786A > G was associated with a significantly worse chemotherapy response and lower overall survival in small cell lung cancer (SCLC). John Wiley & Sons Australia, Ltd 2020-07-22 2020-09 /pmc/articles/PMC7471053/ /pubmed/32700476 http://dx.doi.org/10.1111/1759-7714.13566 Text en © 2020 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Brief Reports Yoo, Seung Soo Lee, Jang Hyuck Hong, Mi Jeong Choi, Jin Eun Kang, Hyo‐Gyoung Do, Sook Kyung Kim, Ji Hyun Baek, Sun Ah Choi, Sun Ha Lee, Won Kee Lee, Yong Hoon Seo, Hyewon Lee, Jaehee Lee, Shin Yup Cha, Seung Ick Kim, Chang Ho Park, Jae Yong Effect of genetic variation in Notch regulator DTX1 on SCLC prognosis compared with the effect on NSCLC prongosis |
title | Effect of genetic variation in Notch regulator DTX1 on SCLC prognosis compared with the effect on NSCLC prongosis |
title_full | Effect of genetic variation in Notch regulator DTX1 on SCLC prognosis compared with the effect on NSCLC prongosis |
title_fullStr | Effect of genetic variation in Notch regulator DTX1 on SCLC prognosis compared with the effect on NSCLC prongosis |
title_full_unstemmed | Effect of genetic variation in Notch regulator DTX1 on SCLC prognosis compared with the effect on NSCLC prongosis |
title_short | Effect of genetic variation in Notch regulator DTX1 on SCLC prognosis compared with the effect on NSCLC prongosis |
title_sort | effect of genetic variation in notch regulator dtx1 on sclc prognosis compared with the effect on nsclc prongosis |
topic | Brief Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7471053/ https://www.ncbi.nlm.nih.gov/pubmed/32700476 http://dx.doi.org/10.1111/1759-7714.13566 |
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