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 in | Cancer Vol. 105; no. 2; pp. 101 - 109 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken
Wiley Subscription Services, Inc., A Wiley Company
25.04.2005
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Online Access | Get full text |
ISSN | 0008-543X 1097-0142 |
DOI | 10.1002/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. |
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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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Cites_doi | 10.1002/cncr.9048 10.1016/S0002-9440(10)63090-8 10.1002/1097-0142(20011115)92:10<2727::AID-CNCR1627>3.0.CO;2-B 10.1186/bcr433 10.1002/cncr.10746 10.1186/1471-2105-3-4 10.1073/pnas.211566398 10.1159/000332774 10.1016/S0002-9440(10)62509-6 10.1073/pnas.87.5.1663 10.1038/sj.onc.1204935 10.1097/00008469-200102000-00009 10.1152/physiolgenomics.2000.2.3.143 10.1093/nar/29.15.e72 |
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References | 2001; 92 2001; 93 2001; 61 1990; 87 2004; 164 2002; 96 1997; 41 2002; 8 2002; 3 2002; 4 2000; 2 2003 2001; 29 2001; 159 2001; 20 2001; 10 2001; 98 Chhieng (10.1002/cncr.20737-BIB3|cit3) 2001; 93 Crnogorac-Jurcevic (10.1002/cncr.20737-BIB9|cit9) 2001; 20 Rubin (10.1002/cncr.20737-BIB1|cit1) 2001; 10 Sotiriou (10.1002/cncr.20737-BIB16|cit16) 2002; 4 Longatto Filho (10.1002/cncr.20737-BIB4|cit4) 1997; 41 Assersohn (10.1002/cncr.20737-BIB15|cit15) 2002; 8 10.1002/cncr.20737-BIB13|cit13 Mills (10.1002/cncr.20737-BIB17|cit17) 2001; 29 Ramaswamy (10.1002/cncr.20737-BIB7|cit7) 2001; 98 Ernst (10.1002/cncr.20737-BIB8|cit8) 2002; 96 10.1002/cncr.20737-BIB12|cit12 Bloom (10.1002/cncr.20737-BIB14|cit14) 2004; 164 Su (10.1002/cncr.20737-BIB6|cit6) 2001; 61 Giordano (10.1002/cncr.20737-BIB5|cit5) 2001; 159 Tot (10.1002/cncr.20737-BIB2|cit2) 2001; 92 Warrington (10.1002/cncr.20737-BIB11|cit11) 2000; 2 Van Gelder (10.1002/cncr.20737-BIB10|cit10) 1990; 87 Bakay (10.1002/cncr.20737-BIB18|cit18) 2002; 3 |
References_xml | – volume: 98 start-page: 15149 year: 2001 end-page: 15154 article-title: Multiclass cancer diagnosis using tumor gene expression signatures publication-title: Proc Natl Acad Sci U S A. – volume: 4 start-page: R3 year: 2002 article-title: Gene expression profiles derived from fine needle aspiration correlate with response to systemic chemotherapy in breast cancer publication-title: Breast Cancer Res. – volume: 87 start-page: 1663 year: 1990 end-page: 1667 article-title: Amplified RNA synthesized from limited quantities of heterogeneous cDNA publication-title: Proc Natl Acad Sci U S A. – volume: 93 start-page: 330 year: 2001 end-page: 336 article-title: Use of thyroid transcription factor 1, PE‐10, and cytokeratins 7 and 20 in discriminating between primary lung carcinomas and metastatic lesions in fine‐needle aspiration biopsy specimens publication-title: Cancer. – volume: 20 start-page: 7437 year: 2001 end-page: 7446 article-title: Gene expression profiles of pancreatic cancer and stromal desmoplasia publication-title: Oncogene. – volume: 92 start-page: 2727 year: 2001 end-page: 2732 article-title: The value of cytokeratins 20 and 7 in discriminating metastatic adenocarcinomas from pleural mesotheliomas publication-title: Cancer. – volume: 159 start-page: 1231 year: 2001 end-page: 1238 article-title: Organ‐specific molecular classification of primary lung, colon, and ovarian adenocarcinomas using gene expression profiles publication-title: Am J Pathol. – volume: 61 start-page: 7388 year: 2001 end-page: 7393 article-title: Molecular classification of human carcinomas by use of gene expression signatures publication-title: Cancer Res. – volume: 2 start-page: 143 year: 2000 end-page: 147 article-title: Comparison of human adult and fetal expression and identification of 535 housekeeping/maintenance genes publication-title: Physiol Genomics. – volume: 164 start-page: 9 year: 2004 end-page: 16 article-title: Multi‐platform, multi‐site, microarray‐based human tumor classification publication-title: Am J Pathol. – year: 2003 – volume: 29 start-page: E72‐2 year: 2001 article-title: A new approach for filtering noise from high‐density oligonucleotide microarray datasets publication-title: Nucleic Acids Res. – volume: 10 start-page: 77 year: 2001 end-page: 82 article-title: Use of cytokeratins 7 and 20 in determining the origin of metastatic carcinoma of unknown primary, with special emphasis on lung cancer publication-title: Eur J Cancer Prev. – volume: 3 start-page: 4 year: 2002 article-title: Sources of variability and effect of experimental approach on expression profiling data interpretation publication-title: BMC Bioinformatics. – volume: 41 start-page: 961 year: 1997 end-page: 971 article-title: Adenocarcinoma in females detected in serous effusions. Cytomorphologic aspects and immunocytochemical reactivity to cytokeratins 7 and 20 publication-title: Acta Cytol. – volume: 96 start-page: 275 year: 2002 end-page: 279 article-title: Quantitative examination of mechanophysical tumor cell enrichment in fine‐needle aspiration specimens publication-title: Cancer. – volume: 8 start-page: 794 year: 2002 end-page: 801 article-title: The feasibility of using fine needle aspiration from primary breast cancers for cDNA microarray analyses publication-title: Clin Cancer Res. – volume: 93 start-page: 330 year: 2001 ident: 10.1002/cncr.20737-BIB3|cit3 article-title: Use of thyroid transcription factor 1, PE-10, and cytokeratins 7 and 20 in discriminating between primary lung carcinomas and metastatic lesions in fine-needle aspiration biopsy specimens publication-title: Cancer. doi: 10.1002/cncr.9048 – volume: 164 start-page: 9 year: 2004 ident: 10.1002/cncr.20737-BIB14|cit14 article-title: Multi-platform, multi-site, microarray-based human tumor classification publication-title: Am J Pathol. doi: 10.1016/S0002-9440(10)63090-8 – volume: 92 start-page: 2727 year: 2001 ident: 10.1002/cncr.20737-BIB2|cit2 article-title: The value of cytokeratins 20 and 7 in discriminating metastatic adenocarcinomas from pleural mesotheliomas publication-title: Cancer. doi: 10.1002/1097-0142(20011115)92:10<2727::AID-CNCR1627>3.0.CO;2-B – volume: 4 start-page: R3 year: 2002 ident: 10.1002/cncr.20737-BIB16|cit16 article-title: Gene expression profiles derived from fine needle aspiration correlate with response to systemic chemotherapy in breast cancer publication-title: Breast Cancer Res. doi: 10.1186/bcr433 – volume: 96 start-page: 275 year: 2002 ident: 10.1002/cncr.20737-BIB8|cit8 article-title: Quantitative examination of mechanophysical tumor cell enrichment in fine-needle aspiration specimens publication-title: Cancer. doi: 10.1002/cncr.10746 – volume: 8 start-page: 794 year: 2002 ident: 10.1002/cncr.20737-BIB15|cit15 article-title: The feasibility of using fine needle aspiration from primary breast cancers for cDNA microarray analyses publication-title: Clin Cancer Res. – ident: 10.1002/cncr.20737-BIB12|cit12 – volume: 3 start-page: 4 year: 2002 ident: 10.1002/cncr.20737-BIB18|cit18 article-title: Sources of variability and effect of experimental approach on expression profiling data interpretation publication-title: BMC Bioinformatics. doi: 10.1186/1471-2105-3-4 – volume: 98 start-page: 15149 year: 2001 ident: 10.1002/cncr.20737-BIB7|cit7 article-title: Multiclass cancer diagnosis using tumor gene expression signatures publication-title: Proc Natl Acad Sci U S A. doi: 10.1073/pnas.211566398 – volume: 41 start-page: 961 year: 1997 ident: 10.1002/cncr.20737-BIB4|cit4 article-title: Adenocarcinoma in females detected in serous effusions. Cytomorphologic aspects and immunocytochemical reactivity to cytokeratins 7 and 20 publication-title: Acta Cytol. doi: 10.1159/000332774 – volume: 159 start-page: 1231 year: 2001 ident: 10.1002/cncr.20737-BIB5|cit5 article-title: Organ-specific molecular classification of primary lung, colon, and ovarian adenocarcinomas using gene expression profiles publication-title: Am J Pathol. doi: 10.1016/S0002-9440(10)62509-6 – volume: 87 start-page: 1663 year: 1990 ident: 10.1002/cncr.20737-BIB10|cit10 article-title: Amplified RNA synthesized from limited quantities of heterogeneous cDNA publication-title: Proc Natl Acad Sci U S A. doi: 10.1073/pnas.87.5.1663 – volume: 20 start-page: 7437 year: 2001 ident: 10.1002/cncr.20737-BIB9|cit9 article-title: Gene expression profiles of pancreatic cancer and stromal desmoplasia publication-title: Oncogene. doi: 10.1038/sj.onc.1204935 – volume: 10 start-page: 77 year: 2001 ident: 10.1002/cncr.20737-BIB1|cit1 article-title: Use of cytokeratins 7 and 20 in determining the origin of metastatic carcinoma of unknown primary, with special emphasis on lung cancer publication-title: Eur J Cancer Prev. doi: 10.1097/00008469-200102000-00009 – volume: 2 start-page: 143 year: 2000 ident: 10.1002/cncr.20737-BIB11|cit11 article-title: Comparison of human adult and fetal expression and identification of 535 housekeeping/maintenance genes publication-title: Physiol Genomics. doi: 10.1152/physiolgenomics.2000.2.3.143 – ident: 10.1002/cncr.20737-BIB13|cit13 – volume: 29 start-page: E72-2 year: 2001 ident: 10.1002/cncr.20737-BIB17|cit17 article-title: A new approach for filtering noise from high-density oligonucleotide microarray datasets publication-title: Nucleic Acids Res. doi: 10.1093/nar/29.15.e72 – volume: 61 start-page: 7388 year: 2001 ident: 10.1002/cncr.20737-BIB6|cit6 article-title: Molecular classification of human carcinomas by use of gene expression signatures publication-title: Cancer Res. |
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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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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 |
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