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An RNA-based signature enables high specificity detection of circulating tumor cells in hepatocellular carcinoma
by
Zhang, Huidan
, Choz, Melissa
, Milner, John D.
, Ting, David T.
, Isselbacher, Kurt J.
, Maheswaran, Shyamala
, Weitz, David A.
, Javaid, Sarah
, Sequist, Lecia V.
, Toner, Mehmet
, Muzikansky, Alona
, Bhan, Irun
, Ho, Uyen
, Kalinich, Mark
, Chung, Raymond T.
, Hong, Xin
, Ryan, David P.
, Goyal, Lipika
, Miyamoto, David T.
, Zhu, Andrew X.
, Haber, Daniel A.
, LiCausi, Joseph A.
, Kwan, Tanya T.
, Sil, Srinjoy
, Kapur, Ravi
in
Biological Sciences
/ Biomarkers, Tumor - blood
/ Blood
/ Carcinoma, Hepatocellular - blood
/ Carcinoma, Hepatocellular - diagnosis
/ Carcinoma, Hepatocellular - pathology
/ Carcinoma, Hepatocellular - therapy
/ Cell Lineage
/ Cell Separation - instrumentation
/ Cell Separation - methods
/ Cells
/ Early Detection of Cancer - methods
/ Gene expression
/ Hep G2 Cells
/ Hepatitis B, Chronic - blood
/ High-Throughput Nucleotide Sequencing - instrumentation
/ High-Throughput Nucleotide Sequencing - methods
/ High-Throughput Screening Assays
/ Humans
/ Lab-On-A-Chip Devices
/ Liver cancer
/ Liver Cirrhosis - blood
/ Liver Neoplasms - blood
/ Liver Neoplasms - diagnosis
/ Liver Neoplasms - pathology
/ Liver Neoplasms - therapy
/ Liver transplantation
/ Logistic Models
/ Medical Sciences
/ Microscopy
/ Neoplastic Cells, Circulating
/ Polymerase chain reaction
/ Precancerous Conditions - blood
/ Predictive Value of Tests
/ Ribonucleic acid
/ RNA
/ RNA, Messenger - blood
/ RNA, Neoplasm - blood
/ Sequence Analysis, RNA - instrumentation
/ Sequence Analysis, RNA - methods
/ Single-Cell Analysis
/ Transcriptome
/ Tumors
2017
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An RNA-based signature enables high specificity detection of circulating tumor cells in hepatocellular carcinoma
by
Zhang, Huidan
, Choz, Melissa
, Milner, John D.
, Ting, David T.
, Isselbacher, Kurt J.
, Maheswaran, Shyamala
, Weitz, David A.
, Javaid, Sarah
, Sequist, Lecia V.
, Toner, Mehmet
, Muzikansky, Alona
, Bhan, Irun
, Ho, Uyen
, Kalinich, Mark
, Chung, Raymond T.
, Hong, Xin
, Ryan, David P.
, Goyal, Lipika
, Miyamoto, David T.
, Zhu, Andrew X.
, Haber, Daniel A.
, LiCausi, Joseph A.
, Kwan, Tanya T.
, Sil, Srinjoy
, Kapur, Ravi
in
Biological Sciences
/ Biomarkers, Tumor - blood
/ Blood
/ Carcinoma, Hepatocellular - blood
/ Carcinoma, Hepatocellular - diagnosis
/ Carcinoma, Hepatocellular - pathology
/ Carcinoma, Hepatocellular - therapy
/ Cell Lineage
/ Cell Separation - instrumentation
/ Cell Separation - methods
/ Cells
/ Early Detection of Cancer - methods
/ Gene expression
/ Hep G2 Cells
/ Hepatitis B, Chronic - blood
/ High-Throughput Nucleotide Sequencing - instrumentation
/ High-Throughput Nucleotide Sequencing - methods
/ High-Throughput Screening Assays
/ Humans
/ Lab-On-A-Chip Devices
/ Liver cancer
/ Liver Cirrhosis - blood
/ Liver Neoplasms - blood
/ Liver Neoplasms - diagnosis
/ Liver Neoplasms - pathology
/ Liver Neoplasms - therapy
/ Liver transplantation
/ Logistic Models
/ Medical Sciences
/ Microscopy
/ Neoplastic Cells, Circulating
/ Polymerase chain reaction
/ Precancerous Conditions - blood
/ Predictive Value of Tests
/ Ribonucleic acid
/ RNA
/ RNA, Messenger - blood
/ RNA, Neoplasm - blood
/ Sequence Analysis, RNA - instrumentation
/ Sequence Analysis, RNA - methods
/ Single-Cell Analysis
/ Transcriptome
/ Tumors
2017
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An RNA-based signature enables high specificity detection of circulating tumor cells in hepatocellular carcinoma
by
Zhang, Huidan
, Choz, Melissa
, Milner, John D.
, Ting, David T.
, Isselbacher, Kurt J.
, Maheswaran, Shyamala
, Weitz, David A.
, Javaid, Sarah
, Sequist, Lecia V.
, Toner, Mehmet
, Muzikansky, Alona
, Bhan, Irun
, Ho, Uyen
, Kalinich, Mark
, Chung, Raymond T.
, Hong, Xin
, Ryan, David P.
, Goyal, Lipika
, Miyamoto, David T.
, Zhu, Andrew X.
, Haber, Daniel A.
, LiCausi, Joseph A.
, Kwan, Tanya T.
, Sil, Srinjoy
, Kapur, Ravi
in
Biological Sciences
/ Biomarkers, Tumor - blood
/ Blood
/ Carcinoma, Hepatocellular - blood
/ Carcinoma, Hepatocellular - diagnosis
/ Carcinoma, Hepatocellular - pathology
/ Carcinoma, Hepatocellular - therapy
/ Cell Lineage
/ Cell Separation - instrumentation
/ Cell Separation - methods
/ Cells
/ Early Detection of Cancer - methods
/ Gene expression
/ Hep G2 Cells
/ Hepatitis B, Chronic - blood
/ High-Throughput Nucleotide Sequencing - instrumentation
/ High-Throughput Nucleotide Sequencing - methods
/ High-Throughput Screening Assays
/ Humans
/ Lab-On-A-Chip Devices
/ Liver cancer
/ Liver Cirrhosis - blood
/ Liver Neoplasms - blood
/ Liver Neoplasms - diagnosis
/ Liver Neoplasms - pathology
/ Liver Neoplasms - therapy
/ Liver transplantation
/ Logistic Models
/ Medical Sciences
/ Microscopy
/ Neoplastic Cells, Circulating
/ Polymerase chain reaction
/ Precancerous Conditions - blood
/ Predictive Value of Tests
/ Ribonucleic acid
/ RNA
/ RNA, Messenger - blood
/ RNA, Neoplasm - blood
/ Sequence Analysis, RNA - instrumentation
/ Sequence Analysis, RNA - methods
/ Single-Cell Analysis
/ Transcriptome
/ Tumors
2017
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An RNA-based signature enables high specificity detection of circulating tumor cells in hepatocellular carcinoma
Journal Article
An RNA-based signature enables high specificity detection of circulating tumor cells in hepatocellular carcinoma
2017
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Overview
Circulating tumor cells (CTCs) are shed into the bloodstream by invasive cancers, but the difficulty inherent in identifying these rare cells by microscopy has precluded their routine use in monitoring or screening for cancer. We recently described a high-throughput microfluidic CTC-iChip, which efficiently depletes hematopoietic cells from blood specimens and enriches for CTCs with well-preserved RNA. Application of RNA-based digital PCR to detect CTC-derived signatures may thus enable highly accurate tissue lineage-based cancer detection in blood specimens. As proof of principle, we examined hepatocellular carcinoma (HCC), a cancer that is derived from liver cells bearing a unique gene expression profile. After identifying a digital signature of 10 liver-specific transcripts, we used a cross-validated logistic regression model to identify the presence of HCC-derived CTCs in nine of 16 (56%) untreated patients with HCC versus one of 31 (3%) patients with nonmalignant liver disease at risk for developing HCC (P < 0.0001). Positive CTC scores declined in treated patients: Nine of 32 (28%) patients receiving therapy and only one of 15 (7%) patients who had undergone curative-intent ablation, surgery, or liver transplantation were positive. RNA-based digital CTC scoring was not correlated with the standard HCC serum protein marker alpha fetoprotein (P = 0.57). Modeling the sequential use of these two orthogonal markers for liver cancer screening in patients with high-risk cirrhosis generates positive and negative predictive values of 80% and 86%, respectively. Thus, digital RNA quantitation constitutes a sensitive and specific CTC readout, enabling high-throughput clinical applications, such as noninvasive screening for HCC in populations where viral hepatitis and cirrhosis are prevalent.
Publisher
National Academy of Sciences
Subject
/ Blood
/ Carcinoma, Hepatocellular - blood
/ Carcinoma, Hepatocellular - diagnosis
/ Carcinoma, Hepatocellular - pathology
/ Carcinoma, Hepatocellular - therapy
/ Cell Separation - instrumentation
/ Cells
/ Early Detection of Cancer - methods
/ Hepatitis B, Chronic - blood
/ High-Throughput Nucleotide Sequencing - instrumentation
/ High-Throughput Nucleotide Sequencing - methods
/ High-Throughput Screening Assays
/ Humans
/ Neoplastic Cells, Circulating
/ Precancerous Conditions - blood
/ RNA
/ Sequence Analysis, RNA - instrumentation
/ Sequence Analysis, RNA - methods
/ Tumors
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