Classification of human tumors using gene expression profiles obtained after microarray analysis of fine‐needle aspiration biopsy samples

BACKGROUND Gene expression profiling using gene‐discovery, high‐density microarray technologies is a powerful tool. One potential application is the development of tumor classifiers that predict the site of origin. For this technology to be relevant, however, it must be applicable to tumor biopsy sa...

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Published inCancer Vol. 105; no. 2; pp. 101 - 109
Main Authors Centeno, Barbara A., Enkemann, Steven A., Coppola, Domenico, Huntsman, Shane, Bloom, Gregory, Yeatman, Timothy J.
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 25.04.2005
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ISSN0008-543X
1097-0142
DOI10.1002/cncr.20737

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Abstract BACKGROUND Gene expression profiling using gene‐discovery, high‐density microarray technologies is a powerful tool. One potential application is the development of tumor classifiers that predict the site of origin. For this technology to be relevant, however, it must be applicable to tumor biopsy samples, which most often are fine‐needle aspiration biopsy (FNAB) samples. METHODS Surgically resected tumors were sampled by FNAB using different gauge needles. A portion of the excised tumor was also collected. RNA samples were extracted using standard techniques and the quality and quantity of the RNA samples were measured for each sample. Thirteen representative FNAB samples and two representative tissue samples were submitted for microarray analysis and then subjected to a tumor classifier. RESULTS Fourteen of 18 samples analyzed for quantity and quality of RNA yielded an adequate amount of RNA (> 1 μg total RNA). Tumor type contributed to the RNA yield because one of the four inadequate samples was retrieved from a patient with lobular carcinoma of the breast and the other three samples were retrieved from patients with retroperitoneal sarcomas. Of the 13 samples submitted for microarray analysis, 9 were classified correctly as to tumor type using a tissue‐based tumor classifier. CONCLUSIONS The authors demonstrated that FNABs reproducibly obtained an adequate amount of RNA for microarray analysis when a standardized collection procedure was used. Furthermore, the samples generated interpretable gene expression profiles that could be matched accurately with a tumor classifier established on tissue specimens. The current study showed that FNAB produced adequate material for microarray analysis when utilizing a standardized collection procedure. Cancer (Cancer Cytopathol) 2005. © 2005 American Cancer Society. Gene expression profiling using gene‐discovery, high‐density microarray technologies is a powerful tool that is used to develop tumor classifiers that predict the site of origin. However, to be clinically relevant, it must be applicable to tumor biopsy samples. The current study demonstrated that fine‐needle aspiration biopsy produced adequate material for microarray analysis and generated interpretable gene expression profiles that can be matched accurately with a tumor classifier established on tissue specimens.
AbstractList Gene expression profiling using gene-discovery, high-density microarray technologies is a powerful tool. One potential application is the development of tumor classifiers that predict the site of origin. For this technology to be relevant, however, it must be applicable to tumor biopsy samples, which most often are fine-needle aspiration biopsy (FNAB) samples. Surgically resected tumors were sampled by FNAB using different gauge needles. A portion of the excised tumor was also collected. RNA samples were extracted using standard techniques and the quality and quantity of the RNA samples were measured for each sample. Thirteen representative FNAB samples and two representative tissue samples were submitted for microarray analysis and then subjected to a tumor classifier. Fourteen of 18 samples analyzed for quantity and quality of RNA yielded an adequate amount of RNA (> 1 microg total RNA). Tumor type contributed to the RNA yield because one of the four inadequate samples was retrieved from a patient with lobular carcinoma of the breast and the other three samples were retrieved from patients with retroperitoneal sarcomas. Of the 13 samples submitted for microarray analysis, 9 were classified correctly as to tumor type using a tissue-based tumor classifier. The authors demonstrated that FNABs reproducibly obtained an adequate amount of RNA for microarray analysis when a standardized collection procedure was used. Furthermore, the samples generated interpretable gene expression profiles that could be matched accurately with a tumor classifier established on tissue specimens. The current study showed that FNAB produced adequate material for microarray analysis when utilizing a standardized collection procedure.
BACKGROUND Gene expression profiling using gene‐discovery, high‐density microarray technologies is a powerful tool. One potential application is the development of tumor classifiers that predict the site of origin. For this technology to be relevant, however, it must be applicable to tumor biopsy samples, which most often are fine‐needle aspiration biopsy (FNAB) samples. METHODS Surgically resected tumors were sampled by FNAB using different gauge needles. A portion of the excised tumor was also collected. RNA samples were extracted using standard techniques and the quality and quantity of the RNA samples were measured for each sample. Thirteen representative FNAB samples and two representative tissue samples were submitted for microarray analysis and then subjected to a tumor classifier. RESULTS Fourteen of 18 samples analyzed for quantity and quality of RNA yielded an adequate amount of RNA (> 1 μg total RNA). Tumor type contributed to the RNA yield because one of the four inadequate samples was retrieved from a patient with lobular carcinoma of the breast and the other three samples were retrieved from patients with retroperitoneal sarcomas. Of the 13 samples submitted for microarray analysis, 9 were classified correctly as to tumor type using a tissue‐based tumor classifier. CONCLUSIONS The authors demonstrated that FNABs reproducibly obtained an adequate amount of RNA for microarray analysis when a standardized collection procedure was used. Furthermore, the samples generated interpretable gene expression profiles that could be matched accurately with a tumor classifier established on tissue specimens. The current study showed that FNAB produced adequate material for microarray analysis when utilizing a standardized collection procedure. Cancer (Cancer Cytopathol) 2005. © 2005 American Cancer Society. Gene expression profiling using gene‐discovery, high‐density microarray technologies is a powerful tool that is used to develop tumor classifiers that predict the site of origin. However, to be clinically relevant, it must be applicable to tumor biopsy samples. The current study demonstrated that fine‐needle aspiration biopsy produced adequate material for microarray analysis and generated interpretable gene expression profiles that can be matched accurately with a tumor classifier established on tissue specimens.
Gene expression profiling using gene-discovery, high-density microarray technologies is a powerful tool. One potential application is the development of tumor classifiers that predict the site of origin. For this technology to be relevant, however, it must be applicable to tumor biopsy samples, which most often are fine-needle aspiration biopsy (FNAB) samples.BACKGROUNDGene expression profiling using gene-discovery, high-density microarray technologies is a powerful tool. One potential application is the development of tumor classifiers that predict the site of origin. For this technology to be relevant, however, it must be applicable to tumor biopsy samples, which most often are fine-needle aspiration biopsy (FNAB) samples.Surgically resected tumors were sampled by FNAB using different gauge needles. A portion of the excised tumor was also collected. RNA samples were extracted using standard techniques and the quality and quantity of the RNA samples were measured for each sample. Thirteen representative FNAB samples and two representative tissue samples were submitted for microarray analysis and then subjected to a tumor classifier.METHODSSurgically resected tumors were sampled by FNAB using different gauge needles. A portion of the excised tumor was also collected. RNA samples were extracted using standard techniques and the quality and quantity of the RNA samples were measured for each sample. Thirteen representative FNAB samples and two representative tissue samples were submitted for microarray analysis and then subjected to a tumor classifier.Fourteen of 18 samples analyzed for quantity and quality of RNA yielded an adequate amount of RNA (> 1 microg total RNA). Tumor type contributed to the RNA yield because one of the four inadequate samples was retrieved from a patient with lobular carcinoma of the breast and the other three samples were retrieved from patients with retroperitoneal sarcomas. Of the 13 samples submitted for microarray analysis, 9 were classified correctly as to tumor type using a tissue-based tumor classifier.RESULTSFourteen of 18 samples analyzed for quantity and quality of RNA yielded an adequate amount of RNA (> 1 microg total RNA). Tumor type contributed to the RNA yield because one of the four inadequate samples was retrieved from a patient with lobular carcinoma of the breast and the other three samples were retrieved from patients with retroperitoneal sarcomas. Of the 13 samples submitted for microarray analysis, 9 were classified correctly as to tumor type using a tissue-based tumor classifier.The authors demonstrated that FNABs reproducibly obtained an adequate amount of RNA for microarray analysis when a standardized collection procedure was used. Furthermore, the samples generated interpretable gene expression profiles that could be matched accurately with a tumor classifier established on tissue specimens. The current study showed that FNAB produced adequate material for microarray analysis when utilizing a standardized collection procedure.CONCLUSIONSThe authors demonstrated that FNABs reproducibly obtained an adequate amount of RNA for microarray analysis when a standardized collection procedure was used. Furthermore, the samples generated interpretable gene expression profiles that could be matched accurately with a tumor classifier established on tissue specimens. The current study showed that FNAB produced adequate material for microarray analysis when utilizing a standardized collection procedure.
Author Enkemann, Steven A.
Centeno, Barbara A.
Huntsman, Shane
Coppola, Domenico
Bloom, Gregory
Yeatman, Timothy J.
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/15643601$$D View this record in MEDLINE/PubMed
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Snippet BACKGROUND Gene expression profiling using gene‐discovery, high‐density microarray technologies is a powerful tool. One potential application is the...
Gene expression profiling using gene-discovery, high-density microarray technologies is a powerful tool. One potential application is the development of tumor...
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StartPage 101
SubjectTerms Biopsy, Fine-Needle
Cell Count
fine‐needle aspiration biopsy
gene expression profile
Gene Expression Profiling
Humans
Microarray Analysis
Neoplasms - classification
RNA
RNA, Messenger - analysis
tumor classifier
Title Classification of human tumors using gene expression profiles obtained after microarray analysis of fine‐needle aspiration biopsy samples
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fcncr.20737
https://www.ncbi.nlm.nih.gov/pubmed/15643601
https://www.proquest.com/docview/67747869
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