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Association between Fusobacterium nucleatum and patient prognosis in metastatic colon cancer

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저자
Jii Bum Lee ; Kyung-A Kim ; Ho Yeon Cho ; DooA Kim ; Won Kyu Kim ; Dongeun Yong ; Hyukmin Lee ; Sang Sun Yoon ; Dai Hoon Han ; Yoon Dae Han ; Soonmyung Paik ; Mi Jang ; Han Sang Kim ; Joong Bae Ahn
키워드 (영문)
cancer microenvironmentcolorectal cancer
발행연도
2021-10
발행기관
Springer
유형
Article
초록
Recent evidence suggests thatFusobacterium nucleatum(Fn) is associated with the development and progression of colorectal cancer. We aimed to delineate the clinical implications ofFnin metastatic colon cancer. We performed quantitative polymerase chain reaction (qPCR) using DNA samples from synchronous metastatic colon cancer patients with either formalin-fixed paraffin-embedded (FFPE) archival primary site tumor samples or fresh colon tissues. Progression-free survival (PFS)1 and PFS2 were defined as PFS of first- and second-line palliative settings. qPCR forFnwas successfully performed using 112 samples (FFPE, n = 61; fresh tissue, n = 51). Forty-one and 68 patients had right-sided and left-sided colon cancer, respectively. Patients withFnenriched right-sided colon cancers had shorter PFS1 (9.7 vs. 11.2 months) than the other subgroups (HR 3.54, 95% confidence interval [CI] 1.05–11.99;P = 0.04).Fnpositive right-sided colon was also associated with shorter PFS2 (3.7 vs. 6.7 months; HR 2.34, 95% CI 0.69–7.91;P = 0.04). In the univariate analysis, PFS1 was affected by differentiation andFnpositive right-sided colon cancer. The multivariate analysis showed that differentiation (HR 2.68, 95% CI 1.40–5.14,P = 0.01) andFnpositive right-sided colon (HR 0.40, 95% CI 0.18–0.88,P = 0.02) were associated with PFS1.Fnenrichment in right sided colon was not associated with overall survival (OS).Fnenrichment has significantly worse prognosis in terms of PFS1 and PFS2 in patients with right-sided metastatic colon cancers.
저널명
Scientific reports
저널정보
(2021-10). Scientific reports, Vol.11(1), 20263–20263
ISSN
0068-1261
EISSN
2045-2322
DOI
10.1038/s41598-021-98941-6
연구주제분류:
NHIMC 학술성과 > 1. 학술논문
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