Cohort profile: The Clinical and Multi-omic (CAMO) cohort, part of the Norwegian Women and Cancer (NOWAC) study

被引:2
作者
Delgado, Andre Berli [1 ]
Tylden, Eline Sol [1 ]
Lukic, Marko [2 ]
Moi, Line [3 ]
Busund, Lill-Tove Rasmussen [1 ,3 ]
Lund, Eiliv [2 ]
Olsen, Karina Standahl [2 ]
机构
[1] UiT Arctic Univ Norway, Fac Hlth Sci, Dept Med Biol, Tromso, Norway
[2] UiT Arctic Univ Norway, Fac Hlth Sci, Dept Community Med, Tromso, Norway
[3] Univ Hosp North Norway, Dept Clin Pathol, Tromso, Norway
来源
PLOS ONE | 2023年 / 18卷 / 02期
基金
欧洲研究理事会;
关键词
BREAST-CANCER; GENE-EXPRESSION; BLOOD;
D O I
10.1371/journal.pone.0281218
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
IntroductionBreast cancer is the most common cancer worldwide and the leading cause of cancer related deaths among women. The high incidence and mortality of breast cancer calls for improved prevention, diagnostics, and treatment, including identification of new prognostic and predictive biomarkers for use in precision medicine. Material and methodsWith the aim of compiling a cohort amenable to integrative study designs, we collected detailed epidemiological and clinical data, blood samples, and tumor tissue from a subset of participants from the prospective, population-based Norwegian Women and Cancer (NOWAC) study. These study participants were diagnosed with invasive breast cancer in North Norway before 2013 according to the Cancer Registry of Norway and constitute the Clinical and Multi-omic (CAMO) cohort. Prospectively collected questionnaire data on lifestyle and reproductive factors and blood samples were extracted from the NOWAC study, clinical and histopathological data were manually curated from medical records, and archived tumor tissue collected. ResultsThe lifestyle and reproductive characteristics of the study participants in the CAMO cohort (n = 388) were largely similar to those of the breast cancer patients in NOWAC (n = 10 356). The majority of the cancers in the CAMO cohort were tumor grade 2 and of the luminal A subtype. Approx. 80% were estrogen receptor positive, 13% were HER2 positive, and 12% were triple negative breast cancers. Lymph node metastases were present in 31% at diagnosis. The epidemiological dataset in the CAMO cohort is complemented by mRNA, miRNA, and metabolomics analyses in plasma, as well as miRNA profiling in tumor tissue. Additionally, histological analyses at the level of proteins and miRNAs in tumor tissue are currently ongoing. ConclusionThe CAMO cohort provides data suitable for epidemiological, clinical, molecular, and multi-omics investigations, thereby enabling a systems epidemiology approach to translational breast cancer research.
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页数:14
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