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Pan-cancer circulating tumor DNA detection in over 10,000 Chinese patients
by
Xu, Yaping
, Li, Lin
, Chang, Lianpeng
, Li, Lifeng
, Zhang, Kai
, Zhang, Yongliang
, Yao, Yu
, Gong, Yan
, Xia, Xuefeng
, Jia, Shuqin
, Zhang, Meng
, Guan, Yanfang
, Zeng, Qiang
in
45
/ 45/23
/ 631/208/514/1948
/ 631/67/69
/ Asian Continental Ancestry Group - genetics
/ Circulating Tumor DNA - analysis
/ Circulating Tumor DNA - blood
/ Circulating Tumor DNA - genetics
/ Clone Cells
/ Cohort Studies
/ Combined treatment
/ Deoxyribonucleic acid
/ DNA
/ DNA sequencing
/ Epidermal growth factor receptors
/ Genetic testing
/ Genome, Human
/ Hematopoiesis
/ Hepatocellular carcinoma
/ Humanities and Social Sciences
/ Humans
/ Leukocytes
/ Leukocytes - metabolism
/ Liver cancer
/ Lung cancer
/ multidisciplinary
/ Mutation
/ Mutation - genetics
/ Neoplasms - blood
/ Neoplasms - genetics
/ Non-small cell lung carcinoma
/ p53 Protein
/ Patients
/ Plasma
/ Prostate cancer
/ Science
/ Science (multidisciplinary)
/ Small cell lung carcinoma
/ Suppressors
/ Therapeutic targets
/ Tumor Burden - genetics
/ Tumors
2021
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Pan-cancer circulating tumor DNA detection in over 10,000 Chinese patients
by
Xu, Yaping
, Li, Lin
, Chang, Lianpeng
, Li, Lifeng
, Zhang, Kai
, Zhang, Yongliang
, Yao, Yu
, Gong, Yan
, Xia, Xuefeng
, Jia, Shuqin
, Zhang, Meng
, Guan, Yanfang
, Zeng, Qiang
in
45
/ 45/23
/ 631/208/514/1948
/ 631/67/69
/ Asian Continental Ancestry Group - genetics
/ Circulating Tumor DNA - analysis
/ Circulating Tumor DNA - blood
/ Circulating Tumor DNA - genetics
/ Clone Cells
/ Cohort Studies
/ Combined treatment
/ Deoxyribonucleic acid
/ DNA
/ DNA sequencing
/ Epidermal growth factor receptors
/ Genetic testing
/ Genome, Human
/ Hematopoiesis
/ Hepatocellular carcinoma
/ Humanities and Social Sciences
/ Humans
/ Leukocytes
/ Leukocytes - metabolism
/ Liver cancer
/ Lung cancer
/ multidisciplinary
/ Mutation
/ Mutation - genetics
/ Neoplasms - blood
/ Neoplasms - genetics
/ Non-small cell lung carcinoma
/ p53 Protein
/ Patients
/ Plasma
/ Prostate cancer
/ Science
/ Science (multidisciplinary)
/ Small cell lung carcinoma
/ Suppressors
/ Therapeutic targets
/ Tumor Burden - genetics
/ Tumors
2021
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Pan-cancer circulating tumor DNA detection in over 10,000 Chinese patients
by
Xu, Yaping
, Li, Lin
, Chang, Lianpeng
, Li, Lifeng
, Zhang, Kai
, Zhang, Yongliang
, Yao, Yu
, Gong, Yan
, Xia, Xuefeng
, Jia, Shuqin
, Zhang, Meng
, Guan, Yanfang
, Zeng, Qiang
in
45
/ 45/23
/ 631/208/514/1948
/ 631/67/69
/ Asian Continental Ancestry Group - genetics
/ Circulating Tumor DNA - analysis
/ Circulating Tumor DNA - blood
/ Circulating Tumor DNA - genetics
/ Clone Cells
/ Cohort Studies
/ Combined treatment
/ Deoxyribonucleic acid
/ DNA
/ DNA sequencing
/ Epidermal growth factor receptors
/ Genetic testing
/ Genome, Human
/ Hematopoiesis
/ Hepatocellular carcinoma
/ Humanities and Social Sciences
/ Humans
/ Leukocytes
/ Leukocytes - metabolism
/ Liver cancer
/ Lung cancer
/ multidisciplinary
/ Mutation
/ Mutation - genetics
/ Neoplasms - blood
/ Neoplasms - genetics
/ Non-small cell lung carcinoma
/ p53 Protein
/ Patients
/ Plasma
/ Prostate cancer
/ Science
/ Science (multidisciplinary)
/ Small cell lung carcinoma
/ Suppressors
/ Therapeutic targets
/ Tumor Burden - genetics
/ Tumors
2021
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Pan-cancer circulating tumor DNA detection in over 10,000 Chinese patients
Journal Article
Pan-cancer circulating tumor DNA detection in over 10,000 Chinese patients
2021
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Overview
Circulating tumor DNA (ctDNA) provides a noninvasive approach to elucidate a patient’s genomic landscape and actionable information. Here, we design a ctDNA-based study of over 10,000 pan-cancer Chinese patients. Using parallel sequencing between plasma and white blood cells, 14% of plasma cell-free DNA samples contain clonal hematopoiesis (CH) variants, for which detectability increases with age. After eliminating CH variants, ctDNA is detected in 73.5% of plasma samples, with small cell lung cancer (91.1%) and prostate cancer (87.9%) showing the highest detectability. The landscape of putative driver genes revealed by ctDNA profiling is similar to that in a tissue-based database (R
2
= 0.87,
p
< 0.001) but also shows some discrepancies, such as higher
EGFR
(44.8% versus 25.2%) and lower
KRAS
(6.8% versus 27.2%) frequencies in non-small cell lung cancer, and a higher
TP53
frequency in hepatocellular carcinoma (53.1% versus 28.6%). Up to 41.2% of plasma samples harbor drug-sensitive alterations. These findings may be helpful for identifying therapeutic targets and combined treatment strategies.
The detection of aberrations in circulating tumour DNA represents a non-invasive method to survey the oncogenes and tumour suppressors that are modified within a patient’s cancer. Here, the authors analysed more than 10,000 patients using a targeted sequencing panel and report on the frequencies of the mutations that they found.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
Subject
/ 45/23
/ Asian Continental Ancestry Group - genetics
/ Circulating Tumor DNA - analysis
/ Circulating Tumor DNA - blood
/ Circulating Tumor DNA - genetics
/ DNA
/ Epidermal growth factor receptors
/ Humanities and Social Sciences
/ Humans
/ Mutation
/ Non-small cell lung carcinoma
/ Patients
/ Plasma
/ Science
/ Tumors
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