Chromosomal instability (CIN) refers to ongoing chromosome segregation errors throughout consecutive cell divisions. CIN is a hallmark of human cancer, and it is associated with poor prognosis, metastasis, and therapeutic resistance. Analyzing CIN of the DNA extracted from cast-off cells in bile samples seems a promising method for diagnosing, monitoring, and predicting the prognosis of biliary tract carcinoma patients. CIN can be assessed using experimental techniques such as bulk DNA sequencing, fluorescence in situ hybridization (FISH), or conventional karyotyping. However, these techniques are either time-consuming or non-specific. The investigators here intend to study whether a new method named Bile Ultrasensitive Chromosomal Aneuploidy Detection (BileCAD), which is based on low-coverage whole-genome sequencing, can be used to analyze CIN and microbial infection analysis thus help diagnosing and treating biliary tract carcinoma patients.
Biliary tract carcinoma account for about 3% of all digestive system tumors, with potential high metastasis and invasion ability. Their early clinical symptoms lack specificity, and they are often found in late stage with poor prognosis. CIN results from errors in chromosome segregation during mitosis, leading to structural and numerical chromosomal abnormalities. It will generate genomic heterogeneity that acts as a substrate for natural selection. Furthermore, it is proved that tumors with aneuploidies and polyploidy resulting from whole-genome doubling are related with metastasis, treatment resistance, and decreased overall survival. It is estimated that 60%-80% of human tumors exhibit chromosomal abnormalities suggestive of CIN. CIN positively correlates with tumor stage and is enriched in relapsed as well as metastatic tumor specimens. Due to the ubiquity of CIN in cancer cells, it is a potentially way to detect CIN in the cast-off cells from the bile samples for diagnosing and monitoring biliary tract carcinoma patients. BileCAD is a new method to detecting CIN in the DNA sample from patients, including extracting DNA from bile, analyzing DNA by low-coverage whole-genome sequencing, processing the data by bio-information techniques, and finally optimizing the management of biliary tract carcinoma patients.The investigators intended to conduct a prospective study by analyzing bile samples from gallbladder cancers and cholangiocarcinoma patients and control groups that without any tumor in the Bile duct and gallbladder or other organs to compare the specificity and sensitivity of BileCAD test for diagnosing biliary tract carcinoma to other modalities, such as pathological diagnosis. At the same time, the consistency of BileCAD microbial analysis results and clinical microbial culture results was compared, so as to provide more reference for clinical diagnosis.
Study Type
OBSERVATIONAL
Enrollment
300
The extracted gDNA from bile sample will be analyzed by BileCAD to determine the level of CINs.
Sir Run Run Shaw Hospital, School of Medicine,Zhejiang University
Hangzhou, Zhejiang, China
RECRUITINGTaizhou First People's Hospital
Taizhou, Zhejiang, China
RECRUITINGTaizhou Hospital of Zhejiang Province
Taizhou, Zhejiang, China
RECRUITINGFirst Affiliated Hospital of Wenzhou Medical University
Wenzhou, Zhejiang, China
RECRUITINGSensitivity of bile sample analysis by BileCADanalysis
Number of patients "declared positive" with the BileCAD test among the patients suffered from biliary tract carcinoma.
Time frame: 12 months
Specificity of bile sample analysis by BileCADanalysis
Number of patients "declared negative" with the BileCAD test among the patients without cancer.
Time frame: 12 months
BileCAD microbial analysis results
Consistency of BileCAD microbial analysis results with clinical microbial culture results
Time frame: 12 months
BileCAD analyzed the sensitivity of different types and locations of malignant tumors
The tumors were classified into different types and sites and the sensitivity of BileCAD to different types and sites of malignant tumors was calculated.
Time frame: 12 months
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