Altered miRNA expression in sputum for diagnosis of non-small cell lung cancer

Analysis of molecular genetic markers in biological fluids has been proposed as a useful tool for cancer diagnosis. MicroRNAs (miRNAs) are small regulatory RNAs that are frequently dysregulated in lung cancer and have shown promise as tissue-based markers for its prognostication. The aim of this stu...

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Published inLung cancer (Amsterdam, Netherlands) Vol. 67; no. 2; pp. 170 - 176
Main Authors Xie, Ying, Todd, Nevins W., Liu, Zhenqiu, Zhan, Min, Fang, HongBin, Peng, Hong, Alattar, Mohammed, Deepak, Janaki, Stass, Sanford A., Jiang, Feng
Format Journal Article
LanguageEnglish
Published Oxford Elsevier Ireland Ltd 01.02.2010
Elsevier
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Online AccessGet full text
ISSN0169-5002
1872-8332
1872-8332
DOI10.1016/j.lungcan.2009.04.004

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Abstract Analysis of molecular genetic markers in biological fluids has been proposed as a useful tool for cancer diagnosis. MicroRNAs (miRNAs) are small regulatory RNAs that are frequently dysregulated in lung cancer and have shown promise as tissue-based markers for its prognostication. The aim of this study was to determine whether aberrant miRNA expression can be used as a marker in sputum specimen for the diagnosis of non-small cell lung cancer (NSCLC). Experimental design: expressions of mature miRNAs, mir-21 and mir-155, were examined by real-time reverse transcription polymerase chain reaction (RT-PCR) and normalized to that of control miRNA, U6B, in sputum of 23 patients with NSCLC and 17 cancer-free subjects. The data was compared with conventional sputum cytology for the diagnosis of lung cancer. All endogenous miRNAs were present in sputum in a remarkably stable form and sensitively and specifically detected by real-time RT-PCR. Mir-21 expression in the sputum specimens was significantly higher in cancer patients (76.32±9.79) than cancer-free individuals (62.24±3.82) (P<0.0001). Furthermore, overexpression of mir-21 showed highly discriminative receiver-operator characteristic (ROC) curve profile, clearly distinguishing cancer patients from cancer-free subjects with areas under the ROC curve at 0.902±0.054. Detection of mir-21 expression produced 69.66% sensitivity and 100.00% specificity in diagnosis of lung cancer, as compared with 47.82% sensitivity and 100.00% specificity by sputum cytology. The measurement of altered miRNA expression in sputum could be a useful noninvasive approach for the diagnosis of lung cancer.
AbstractList Analysis of molecular genetic markers in biological fluids has been proposed as a useful tool for cancer diagnosis. MicroRNAs (miRNAs) are small regulatory RNAs that are frequently dysregulated in lung cancer and have shown promise as tissue-based markers for its prognostication. The aim of this study was to determine whether aberrant miRNA expression can be used as a marker in sputum specimen for the diagnosis of non-small cell lung cancer (NSCLC). expressions of mature miRNAs, mir-21 and mir-155, were examined by real-time reverse transcription polymerase chain reaction (RT-PCR) and normalized to that of control miRNA, U6B, in sputum of 23 patients with NSCLC and 17 cancer-free subjects. The data was compared with conventional sputum cytology for the diagnosis of lung cancer. All endogenous miRNAs were present in sputum in a remarkably stable form and sensitively and specifically detected by real-time RT-PCR. Mir-21 expression in the sputum specimens was significantly higher in cancer patients (76.32+/-9.79) than cancer-free individuals (62.24+/-3.82) (P<0.0001). Furthermore, overexpression of mir-21 showed highly discriminative receiver-operator characteristic (ROC) curve profile, clearly distinguishing cancer patients from cancer-free subjects with areas under the ROC curve at 0.902+/-0.054. Detection of mir-21 expression produced 69.66% sensitivity and 100.00% specificity in diagnosis of lung cancer, as compared with 47.82% sensitivity and 100.00% specificity by sputum cytology. The measurement of altered miRNA expression in sputum could be a useful noninvasive approach for the diagnosis of lung cancer.
Analysis of molecular genetic markers in biological fluids has been proposed as a useful tool for cancer diagnosis. MicroRNAs (miRNAs) are small regulatory RNAs that are frequently dysregulated in lung cancer and have shown promise as tissue-based markers for its prognostication. The aim of this study was to determine whether aberrant miRNA expression can be used as a marker in sputum specimen for the diagnosis of non-small cell lung cancer (NSCLC). Experimental Design: Expressions of mature miRNAs , mir-21 and mir-155, were examined by real-time reverse transcription polymerase chain reaction (RT-PCR) and normalized to that of control miRNA, U6B, in sputum of 23 patients with NSCLC and 17 cancer-free subjects. The data was compared with conventional sputum cytology for the diagnosis of lung cancer. All endogenous miRNAs were present in sputum in a remarkably stable form and sensitively and specifically detected by real-time RT-PCR. Mir-21 expression in the sputum specimens was significantly higher in cancer patients (76.32 ± 9.79) than cancer-free individuals (62.24±3.82) (p<0.0001). Furthermore, overexpression of mir-21 showed highly discriminative receiver-operator characteristic (ROC) curve profile, clearly distinguishing cancer patients from cancer-free subjects with areas under the ROC curve at 0.902 ± 0.054. Detection of mir-21 expression produced 69.66% sensitivity and 100.00% specificity in diagnosis of lung cancer, as compared with 47.82% sensitivity and 100.00% specificity by sputum cytology. The measurement of altered miRNA expression in sputum could be a useful noninvasive approach for the diagnosis of lung cancer.
Analysis of molecular genetic markers in biological fluids has been proposed as a useful tool for cancer diagnosis. MicroRNAs (miRNAs) are small regulatory RNAs that are frequently dysregulated in lung cancer and have shown promise as tissue-based markers for its prognostication. The aim of this study was to determine whether aberrant miRNA expression can be used as a marker in sputum specimen for the diagnosis of non-small cell lung cancer (NSCLC).UNLABELLEDAnalysis of molecular genetic markers in biological fluids has been proposed as a useful tool for cancer diagnosis. MicroRNAs (miRNAs) are small regulatory RNAs that are frequently dysregulated in lung cancer and have shown promise as tissue-based markers for its prognostication. The aim of this study was to determine whether aberrant miRNA expression can be used as a marker in sputum specimen for the diagnosis of non-small cell lung cancer (NSCLC).expressions of mature miRNAs, mir-21 and mir-155, were examined by real-time reverse transcription polymerase chain reaction (RT-PCR) and normalized to that of control miRNA, U6B, in sputum of 23 patients with NSCLC and 17 cancer-free subjects. The data was compared with conventional sputum cytology for the diagnosis of lung cancer. All endogenous miRNAs were present in sputum in a remarkably stable form and sensitively and specifically detected by real-time RT-PCR. Mir-21 expression in the sputum specimens was significantly higher in cancer patients (76.32+/-9.79) than cancer-free individuals (62.24+/-3.82) (P<0.0001). Furthermore, overexpression of mir-21 showed highly discriminative receiver-operator characteristic (ROC) curve profile, clearly distinguishing cancer patients from cancer-free subjects with areas under the ROC curve at 0.902+/-0.054. Detection of mir-21 expression produced 69.66% sensitivity and 100.00% specificity in diagnosis of lung cancer, as compared with 47.82% sensitivity and 100.00% specificity by sputum cytology. The measurement of altered miRNA expression in sputum could be a useful noninvasive approach for the diagnosis of lung cancer.EXPERIMENTAL DESIGNexpressions of mature miRNAs, mir-21 and mir-155, were examined by real-time reverse transcription polymerase chain reaction (RT-PCR) and normalized to that of control miRNA, U6B, in sputum of 23 patients with NSCLC and 17 cancer-free subjects. The data was compared with conventional sputum cytology for the diagnosis of lung cancer. All endogenous miRNAs were present in sputum in a remarkably stable form and sensitively and specifically detected by real-time RT-PCR. Mir-21 expression in the sputum specimens was significantly higher in cancer patients (76.32+/-9.79) than cancer-free individuals (62.24+/-3.82) (P<0.0001). Furthermore, overexpression of mir-21 showed highly discriminative receiver-operator characteristic (ROC) curve profile, clearly distinguishing cancer patients from cancer-free subjects with areas under the ROC curve at 0.902+/-0.054. Detection of mir-21 expression produced 69.66% sensitivity and 100.00% specificity in diagnosis of lung cancer, as compared with 47.82% sensitivity and 100.00% specificity by sputum cytology. The measurement of altered miRNA expression in sputum could be a useful noninvasive approach for the diagnosis of lung cancer.
Analysis of molecular genetic markers in biological fluids has been proposed as a useful tool for cancer diagnosis. MicroRNAs (miRNAs) are small regulatory RNAs that are frequently dysregulated in lung cancer and have shown promise as tissue-based markers for its prognostication. The aim of this study was to determine whether aberrant miRNA expression can be used as a marker in sputum specimen for the diagnosis of non-small cell lung cancer (NSCLC). Experimental design: expressions of mature miRNAs, mir-21 and mir-155, were examined by real-time reverse transcription polymerase chain reaction (RT-PCR) and normalized to that of control miRNA, U6B, in sputum of 23 patients with NSCLC and 17 cancer-free subjects. The data was compared with conventional sputum cytology for the diagnosis of lung cancer. All endogenous miRNAs were present in sputum in a remarkably stable form and sensitively and specifically detected by real-time RT-PCR. Mir-21 expression in the sputum specimens was significantly higher in cancer patients (76.32±9.79) than cancer-free individuals (62.24±3.82) (P<0.0001). Furthermore, overexpression of mir-21 showed highly discriminative receiver-operator characteristic (ROC) curve profile, clearly distinguishing cancer patients from cancer-free subjects with areas under the ROC curve at 0.902±0.054. Detection of mir-21 expression produced 69.66% sensitivity and 100.00% specificity in diagnosis of lung cancer, as compared with 47.82% sensitivity and 100.00% specificity by sputum cytology. The measurement of altered miRNA expression in sputum could be a useful noninvasive approach for the diagnosis of lung cancer.
Abstract Analysis of molecular genetic markers in biological fluids has been proposed as a useful tool for cancer diagnosis. MicroRNAs (miRNAs) are small regulatory RNAs that are frequently dysregulated in lung cancer and have shown promise as tissue-based markers for its prognostication. The aim of this study was to determine whether aberrant miRNA expression can be used as a marker in sputum specimen for the diagnosis of non-small cell lung cancer (NSCLC). Experimental design: expressions of mature miRNAs, mir-21 and mir-155 , were examined by real-time reverse transcription polymerase chain reaction (RT-PCR) and normalized to that of control miRNA, U6B , in sputum of 23 patients with NSCLC and 17 cancer-free subjects. The data was compared with conventional sputum cytology for the diagnosis of lung cancer. All endogenous miRNAs were present in sputum in a remarkably stable form and sensitively and specifically detected by real-time RT-PCR. Mir-21 expression in the sputum specimens was significantly higher in cancer patients (76.32 ± 9.79) than cancer-free individuals (62.24 ± 3.82) ( P < 0.0001). Furthermore, overexpression of mir-21 showed highly discriminative receiver-operator characteristic (ROC) curve profile, clearly distinguishing cancer patients from cancer-free subjects with areas under the ROC curve at 0.902 ± 0.054. Detection of mir-21 expression produced 69.66% sensitivity and 100.00% specificity in diagnosis of lung cancer, as compared with 47.82% sensitivity and 100.00% specificity by sputum cytology. The measurement of altered miRNA expression in sputum could be a useful noninvasive approach for the diagnosis of lung cancer.
Author Todd, Nevins W.
Peng, Hong
Stass, Sanford A.
Jiang, Feng
Alattar, Mohammed
Liu, Zhenqiu
Zhan, Min
Xie, Ying
Fang, HongBin
Deepak, Janaki
AuthorAffiliation 4 Epidemiology and Preventive Medicine, University of Maryland School of Medicine, Baltimore, MD
2 Department of Medicine, University of Maryland School of Medicine, Baltimore, MD
1 Department of Pathology, University of Maryland School of Medicine, Baltimore, MD
3 Division of Biostatistics of The University of Maryland Greenebaum Cancer Center, University of Maryland School of Medicine, Baltimore, MD
AuthorAffiliation_xml – name: 1 Department of Pathology, University of Maryland School of Medicine, Baltimore, MD
– name: 3 Division of Biostatistics of The University of Maryland Greenebaum Cancer Center, University of Maryland School of Medicine, Baltimore, MD
– name: 4 Epidemiology and Preventive Medicine, University of Maryland School of Medicine, Baltimore, MD
– name: 2 Department of Medicine, University of Maryland School of Medicine, Baltimore, MD
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  surname: Xie
  fullname: Xie, Ying
  organization: Department of Pathology, University of Maryland School of Medicine, Baltimore, MD, USA
– sequence: 2
  givenname: Nevins W.
  surname: Todd
  fullname: Todd, Nevins W.
  organization: Department of Medicine, University of Maryland School of Medicine, Baltimore, MD, USA
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  givenname: Zhenqiu
  surname: Liu
  fullname: Liu, Zhenqiu
  organization: Division of Biostatistics of The University of Maryland Greenebaum Cancer Center, University of Maryland School of Medicine, Baltimore, MD, USA
– sequence: 4
  givenname: Min
  surname: Zhan
  fullname: Zhan, Min
  organization: Department of Epidemiology and Preventive Medicine, University of Maryland School of Medicine, Baltimore, MD, USA
– sequence: 5
  givenname: HongBin
  surname: Fang
  fullname: Fang, HongBin
  organization: Division of Biostatistics of The University of Maryland Greenebaum Cancer Center, University of Maryland School of Medicine, Baltimore, MD, USA
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  surname: Peng
  fullname: Peng, Hong
  organization: Department of Pathology, University of Maryland School of Medicine, Baltimore, MD, USA
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  givenname: Mohammed
  surname: Alattar
  fullname: Alattar, Mohammed
  organization: Department of Medicine, University of Maryland School of Medicine, Baltimore, MD, USA
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  surname: Deepak
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  organization: Department of Medicine, University of Maryland School of Medicine, Baltimore, MD, USA
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  givenname: Feng
  surname: Jiang
  fullname: Jiang, Feng
  email: fjiang@som.umaryland.edu
  organization: Department of Pathology, University of Maryland School of Medicine, Baltimore, MD, USA
BackLink http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22350990$$DView record in Pascal Francis
https://www.ncbi.nlm.nih.gov/pubmed/19446359$$D View this record in MEDLINE/PubMed
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Cites_doi 10.1158/0008-5472.CAN-05-0137
10.3322/canjclin.51.1.15
10.1093/nar/gni178
10.1002/cncr.23596
10.1073/pnas.0703942104
10.1016/j.ajhg.2008.04.005
10.1073/pnas.0804549105
10.1016/j.ccr.2006.01.025
10.1158/0008-5472.CAN-04-0637
10.1136/jcp.56.11.805
10.2174/092986709787581833
10.1210/jc.2007-2696
10.1126/science.1064921
10.1016/S1535-6108(02)00027-2
10.1158/1078-0432.CCR-06-1593
10.1378/chest.123.1_suppl.137S
10.1002/1097-0142(197401)33:1<256::AID-CNCR2820330139>3.0.CO;2-G
10.1373/clinchem.2007.101741
10.1074/jbc.M611393200
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Issue 2
Keywords Real-time RT-PCR
MicroRNA
Diagnosis
Lung cancer
Sputum
Lung disease
Respiratory disease
Malignant tumor
non-small cell lung carcinoma
Gene expression
Real time
Cancerology
Bronchus disease
Molecular biology
Reverse transcription polymerase chain reaction
Cancer
Pneumology
Language English
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CC BY 4.0
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References Greenlee, Hill-Harmon, Murray, Thun (bib1) 2001; 51
Hirsch, Franklin, Gazdar, Bunn (bib3) 2001; 7
Toloza, Harpole, McCrory (bib4) 2003; 123
Ortholan, Puissegur, Ilie, Barbry, Mari, Hofman (bib12) 2009; 16
Li, Todd, Qiu, Fan, Zhao, Rodgers (bib8) 2007; 13
Saccomanno, Archer, Auerbach, Saunders, Brennan (bib6) 1974; 33
Zhu, Si, Wu, Mo (bib19) 2007; 282
Mitchell, Parkin, Kroh, Fritz, Wyman, Pogosova-Agadjanyan (bib16) 2008; 105
Gironella, Seux, Xie, Cano, Tomasini, Gommeaux (bib20) 2007; 104
Qiu, Todd, Li, Peng, Liu, Yfantis, Katz, Stass, Jiang (bib9) 2008; 114
Takamizawa, Konishi, Yanagisawa, Tomida, Osada, Endoh (bib13) 2004; 64
Lagos-Quintana, Rauhut, Lendeckel, Tuschl (bib10) 2001; 294
Flehinger, Melamed, Zaman, Heelan, Perchick, Martini (bib2) 1984; 130
Thunnissen (bib7) 2003; 11
Nikiforova, Tseng, Steward, Diorio, Nikiforov (bib21) 2008; 93
Markou, Tsaroucha, Kaklamanis, Fotinou, Georgoulias, Lianidou (bib14) 2008; 54
Minna, Roth, Gazdar (bib5) 2002; 1
Yanaihara, Caplen, Bowman, Seike, Kumamoto, Yi (bib11) 2006; 9
Chen, Ridzon, Broomer, Zhou, Lee, Nguyen (bib15) 2005; 33
Chan, Krichevsky, Kosik (bib17) 2005; 65
Pezzolesi, Platzer, Waite, Eng (bib18) 2008; 82
Toloza (10.1016/j.lungcan.2009.04.004_bib4) 2003; 123
Minna (10.1016/j.lungcan.2009.04.004_bib5) 2002; 1
Pezzolesi (10.1016/j.lungcan.2009.04.004_bib18) 2008; 82
Gironella (10.1016/j.lungcan.2009.04.004_bib20) 2007; 104
Nikiforova (10.1016/j.lungcan.2009.04.004_bib21) 2008; 93
Markou (10.1016/j.lungcan.2009.04.004_bib14) 2008; 54
Zhu (10.1016/j.lungcan.2009.04.004_bib19) 2007; 282
Hirsch (10.1016/j.lungcan.2009.04.004_bib3) 2001; 7
Takamizawa (10.1016/j.lungcan.2009.04.004_bib13) 2004; 64
Greenlee (10.1016/j.lungcan.2009.04.004_bib1) 2001; 51
Li (10.1016/j.lungcan.2009.04.004_bib8) 2007; 13
Ortholan (10.1016/j.lungcan.2009.04.004_bib12) 2009; 16
Qiu (10.1016/j.lungcan.2009.04.004_bib9) 2008; 114
Flehinger (10.1016/j.lungcan.2009.04.004_bib2) 1984; 130
Chen (10.1016/j.lungcan.2009.04.004_bib15) 2005; 33
Lagos-Quintana (10.1016/j.lungcan.2009.04.004_bib10) 2001; 294
Chan (10.1016/j.lungcan.2009.04.004_bib17) 2005; 65
Thunnissen (10.1016/j.lungcan.2009.04.004_bib7) 2003; 11
Yanaihara (10.1016/j.lungcan.2009.04.004_bib11) 2006; 9
Mitchell (10.1016/j.lungcan.2009.04.004_bib16) 2008; 105
Saccomanno (10.1016/j.lungcan.2009.04.004_bib6) 1974; 33
References_xml – volume: 294
  start-page: 853
  year: 2001
  end-page: 858
  ident: bib10
  article-title: Identification of novel genes coding for small expressed RNAs
  publication-title: Science
– volume: 282
  start-page: 14328
  year: 2007
  end-page: 14336
  ident: bib19
  article-title: MicroRNA-21 targets the tumor suppressor gene tropomyosin 1 (TPM1)
  publication-title: J Biol Chem
– volume: 104
  start-page: 16170
  year: 2007
  end-page: 16175
  ident: bib20
  article-title: Tumor protein 53-induced nuclear protein 1 expression is repressed by
  publication-title: Proc Natl Acad Sci USA
– volume: 51
  start-page: 15
  year: 2001
  end-page: 36
  ident: bib1
  article-title: Cancer statistics, 2001
  publication-title: CA Cancer J Clin
– volume: 65
  start-page: 6029
  year: 2005
  end-page: 6033
  ident: bib17
  article-title: MicroRNA-21 is an antiapoptotic factor in human glioblastoma cells
  publication-title: Cancer Res
– volume: 9
  start-page: 189
  year: 2006
  end-page: 198
  ident: bib11
  article-title: Unique microRNA molecular profiles in lung cancer diagnosis and prognosis
  publication-title: Cancer Cell
– volume: 54
  start-page: 1696
  year: 2008
  end-page: 1704
  ident: bib14
  article-title: Prognostic value of mature microRNA-21 and microRNA-205 overexpression in non-small cell lung cancer by quantitative real-time RT-PCR
  publication-title: Clin Chem
– volume: 13
  start-page: 482
  year: 2007
  end-page: 487
  ident: bib8
  article-title: Genetic deletions in sputum as diagnostic markers for early detection of stage I non-small cell lung cancer
  publication-title: Clin Cancer Res
– volume: 64
  start-page: 3753
  year: 2004
  end-page: 3756
  ident: bib13
  article-title: Reduced expression of the let-7 microRNAs in human lung cancers in association with shortened postoperative survival
  publication-title: Cancer Res
– volume: 130
  start-page: 549
  year: 1984
  end-page: 554
  ident: bib2
  article-title: Early lung cancer detection: results of the initial (prevalence) radiologic and cytologic screening in the Johns Hopkins study
  publication-title: Am Rev Respir Dis
– volume: 123
  start-page: 137S
  year: 2003
  end-page: 146S
  ident: bib4
  article-title: Noninvasive staging of non-small cell lung cancer: a review of the current evidence
  publication-title: Chest
– volume: 93
  start-page: 1600
  year: 2008
  end-page: 1608
  ident: bib21
  article-title: MicroRNA expression profiling of thyroid tumors: biological significance and diagnostic utility
  publication-title: J Clin Endocrinol Metab
– volume: 105
  start-page: 10513
  year: 2008
  end-page: 10518
  ident: bib16
  article-title: Circulating microRNAs as stable blood-based markers for cancer detection
  publication-title: Proc Natl Acad Sci USA
– volume: 82
  start-page: 1141
  year: 2008
  end-page: 1149
  ident: bib18
  article-title: Differential expression of PTEN-targeting microRNAs
  publication-title: Am J Hum Genet
– volume: 11
  start-page: 805
  year: 2003
  end-page: 810
  ident: bib7
  article-title: Sputum examination for early detection of lung cancer
  publication-title: J Clin Pathol
– volume: 33
  start-page: e179
  year: 2005
  ident: bib15
  article-title: Real-time quantification of microRNAs by stem-loop RT-PCR
  publication-title: Nucleic Acids Res
– volume: 33
  start-page: 256
  year: 1974
  end-page: 270
  ident: bib6
  article-title: Development of carcinoma of the lung as reflected in exfoliated cells
  publication-title: Cancer
– volume: 16
  start-page: 1047
  year: 2009
  end-page: 1061
  ident: bib12
  article-title: MicroRNAs and Lung Cancer: New Oncogenes and Tumor Suppressors, New Prognostic Factors and Potential Therapeutic Targets
  publication-title: Curr Med Chem
– volume: 7
  start-page: 5
  year: 2001
  end-page: 22
  ident: bib3
  article-title: Early detection of lung cancer: clinical perspectives of recent advances in biology and radiology
  publication-title: Clin Cancer Res
– volume: 114
  start-page: 275
  year: 2008
  end-page: 283
  ident: bib9
  article-title: Magnetic enrichment of bronchial epithelial cells from sputum for lung cancer diagnosis
  publication-title: Cancer
– volume: 1
  start-page: 49
  year: 2002
  end-page: 52
  ident: bib5
  article-title: Focus on lung cancer
  publication-title: Cancer Cell
– volume: 65
  start-page: 6029
  year: 2005
  ident: 10.1016/j.lungcan.2009.04.004_bib17
  article-title: MicroRNA-21 is an antiapoptotic factor in human glioblastoma cells
  publication-title: Cancer Res
  doi: 10.1158/0008-5472.CAN-05-0137
– volume: 51
  start-page: 15
  year: 2001
  ident: 10.1016/j.lungcan.2009.04.004_bib1
  article-title: Cancer statistics, 2001
  publication-title: CA Cancer J Clin
  doi: 10.3322/canjclin.51.1.15
– volume: 33
  start-page: e179
  year: 2005
  ident: 10.1016/j.lungcan.2009.04.004_bib15
  article-title: Real-time quantification of microRNAs by stem-loop RT-PCR
  publication-title: Nucleic Acids Res
  doi: 10.1093/nar/gni178
– volume: 130
  start-page: 549
  year: 1984
  ident: 10.1016/j.lungcan.2009.04.004_bib2
  article-title: Early lung cancer detection: results of the initial (prevalence) radiologic and cytologic screening in the Johns Hopkins study
  publication-title: Am Rev Respir Dis
– volume: 114
  start-page: 275
  year: 2008
  ident: 10.1016/j.lungcan.2009.04.004_bib9
  article-title: Magnetic enrichment of bronchial epithelial cells from sputum for lung cancer diagnosis
  publication-title: Cancer
  doi: 10.1002/cncr.23596
– volume: 104
  start-page: 16170
  year: 2007
  ident: 10.1016/j.lungcan.2009.04.004_bib20
  article-title: Tumor protein 53-induced nuclear protein 1 expression is repressed by miR-155, and its restoration inhibits pancreatic tumor development
  publication-title: Proc Natl Acad Sci USA
  doi: 10.1073/pnas.0703942104
– volume: 82
  start-page: 1141
  year: 2008
  ident: 10.1016/j.lungcan.2009.04.004_bib18
  article-title: Differential expression of PTEN-targeting microRNAs miR-19a and miR-21 in Cowden syndrome
  publication-title: Am J Hum Genet
  doi: 10.1016/j.ajhg.2008.04.005
– volume: 105
  start-page: 10513
  year: 2008
  ident: 10.1016/j.lungcan.2009.04.004_bib16
  article-title: Circulating microRNAs as stable blood-based markers for cancer detection
  publication-title: Proc Natl Acad Sci USA
  doi: 10.1073/pnas.0804549105
– volume: 9
  start-page: 189
  year: 2006
  ident: 10.1016/j.lungcan.2009.04.004_bib11
  article-title: Unique microRNA molecular profiles in lung cancer diagnosis and prognosis
  publication-title: Cancer Cell
  doi: 10.1016/j.ccr.2006.01.025
– volume: 64
  start-page: 3753
  year: 2004
  ident: 10.1016/j.lungcan.2009.04.004_bib13
  article-title: Reduced expression of the let-7 microRNAs in human lung cancers in association with shortened postoperative survival
  publication-title: Cancer Res
  doi: 10.1158/0008-5472.CAN-04-0637
– volume: 11
  start-page: 805
  year: 2003
  ident: 10.1016/j.lungcan.2009.04.004_bib7
  article-title: Sputum examination for early detection of lung cancer
  publication-title: J Clin Pathol
  doi: 10.1136/jcp.56.11.805
– volume: 16
  start-page: 1047
  year: 2009
  ident: 10.1016/j.lungcan.2009.04.004_bib12
  article-title: MicroRNAs and Lung Cancer: New Oncogenes and Tumor Suppressors, New Prognostic Factors and Potential Therapeutic Targets
  publication-title: Curr Med Chem
  doi: 10.2174/092986709787581833
– volume: 93
  start-page: 1600
  year: 2008
  ident: 10.1016/j.lungcan.2009.04.004_bib21
  article-title: MicroRNA expression profiling of thyroid tumors: biological significance and diagnostic utility
  publication-title: J Clin Endocrinol Metab
  doi: 10.1210/jc.2007-2696
– volume: 294
  start-page: 853
  year: 2001
  ident: 10.1016/j.lungcan.2009.04.004_bib10
  article-title: Identification of novel genes coding for small expressed RNAs
  publication-title: Science
  doi: 10.1126/science.1064921
– volume: 7
  start-page: 5
  year: 2001
  ident: 10.1016/j.lungcan.2009.04.004_bib3
  article-title: Early detection of lung cancer: clinical perspectives of recent advances in biology and radiology
  publication-title: Clin Cancer Res
– volume: 1
  start-page: 49
  year: 2002
  ident: 10.1016/j.lungcan.2009.04.004_bib5
  article-title: Focus on lung cancer
  publication-title: Cancer Cell
  doi: 10.1016/S1535-6108(02)00027-2
– volume: 13
  start-page: 482
  year: 2007
  ident: 10.1016/j.lungcan.2009.04.004_bib8
  article-title: Genetic deletions in sputum as diagnostic markers for early detection of stage I non-small cell lung cancer
  publication-title: Clin Cancer Res
  doi: 10.1158/1078-0432.CCR-06-1593
– volume: 123
  start-page: 137S
  year: 2003
  ident: 10.1016/j.lungcan.2009.04.004_bib4
  article-title: Noninvasive staging of non-small cell lung cancer: a review of the current evidence
  publication-title: Chest
  doi: 10.1378/chest.123.1_suppl.137S
– volume: 33
  start-page: 256
  year: 1974
  ident: 10.1016/j.lungcan.2009.04.004_bib6
  article-title: Development of carcinoma of the lung as reflected in exfoliated cells
  publication-title: Cancer
  doi: 10.1002/1097-0142(197401)33:1<256::AID-CNCR2820330139>3.0.CO;2-G
– volume: 54
  start-page: 1696
  year: 2008
  ident: 10.1016/j.lungcan.2009.04.004_bib14
  article-title: Prognostic value of mature microRNA-21 and microRNA-205 overexpression in non-small cell lung cancer by quantitative real-time RT-PCR
  publication-title: Clin Chem
  doi: 10.1373/clinchem.2007.101741
– volume: 282
  start-page: 14328
  year: 2007
  ident: 10.1016/j.lungcan.2009.04.004_bib19
  article-title: MicroRNA-21 targets the tumor suppressor gene tropomyosin 1 (TPM1)
  publication-title: J Biol Chem
  doi: 10.1074/jbc.M611393200
SSID ssj0017109
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Snippet Analysis of molecular genetic markers in biological fluids has been proposed as a useful tool for cancer diagnosis. MicroRNAs (miRNAs) are small regulatory...
Abstract Analysis of molecular genetic markers in biological fluids has been proposed as a useful tool for cancer diagnosis. MicroRNAs (miRNAs) are small...
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StartPage 170
SubjectTerms Aged
Area Under Curve
Biological and medical sciences
Biomarkers, Tumor - analysis
Carcinoma, Non-Small-Cell Lung - diagnosis
Carcinoma, Non-Small-Cell Lung - genetics
Diagnosis
Female
Hematology, Oncology and Palliative Medicine
Humans
Lung cancer
Lung Neoplasms - diagnosis
Lung Neoplasms - genetics
Male
Medical sciences
MicroRNA
MicroRNAs - analysis
Neoplasm Staging
Pneumology
Pulmonary/Respiratory
Real-time RT-PCR
Reverse Transcriptase Polymerase Chain Reaction
RNA Stability
ROC Curve
Sensitivity and Specificity
Sputum
Sputum - cytology
Sputum - metabolism
Tumors
Tumors of the respiratory system and mediastinum
Title Altered miRNA expression in sputum for diagnosis of non-small cell lung cancer
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https://www.clinicalkey.es/playcontent/1-s2.0-S0169500209002153
https://dx.doi.org/10.1016/j.lungcan.2009.04.004
https://www.ncbi.nlm.nih.gov/pubmed/19446359
https://www.proquest.com/docview/733836890
https://pubmed.ncbi.nlm.nih.gov/PMC2846426
Volume 67
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