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We are analyzing https://link.springer.com/article/10.1186/1756-9966-29-75.

Title:
MicroRNA expression distinguishes SCLC from NSCLC lung tumor cells and suggests a possible pathological relationship between SCLCs and NSCLCs | Journal of Experimental & Clinical Cancer Research
Description:
Background Recent studies have shown that microRNAs (miRNAs) play roles in tumorigenesis and are reliable classifiers of certain cancer types and subtypes. However, the role of miRNAs in the pathogenesis and diagnosis of small cell carcinoma (SCLC), the majority of which represent the most aggressive lung tumors, has not been investigated. Methods In order to explore miRNA involvement in the pathogenesis of small cell lung carcinoma (SCLC) and the potential role of miRNAs in SCLC diagnosis, we compared the miRNA expression profile of a set of SCLC cell lines to that of a set of non-small cell lung cancer (NSCLC) cell lines and normal immortalized human bronchial epithelial cells (HBECs) using microarray analysis. Results Our results show that miRNA profiles reliably distinguish SCLC cell lines from NSCLC and HBEC cell lines. Further analysis of the miRNA expression profile of the two subtypes of lung cancer cell lines indicates that the expression levels of the majority of the miRNAs that are differentially expressed in SCLC cells relative to NSCLC cells and HBECs show a progressive trend from HBECs to NSCLC cells to SCLC cells. Conclusions The distinctive miRNA expression signature of SCLCs relative to NSCLCs and HBECs suggests that miRNA profiles have the potential to serve as a diagnostic marker of SCLC lung tumors. The progressive trend of miRNA profile changes from HBECs to NSCLCs to SCLCs suggests a possible pathological relationship between SCLCs and NSCLCs, and suggests that the increasing dysregulation of miRNA expression may play a role in lung tumor progression. The specific role of these miRNAs in lung tumor pathogenesis and differentiation need to be investigated further in future studies.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {πŸ“š}

  • Education
  • Telecommunications
  • Health & Fitness

Content Management System {πŸ“}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {πŸ“ˆ}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 7,626,432 visitors per month in the current month.

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How Does Link.springer.com Make Money? {πŸ’Έ}

We can't tell how the site generates income.

The purpose of some websites isn't monetary gain; they're meant to inform, educate, or foster collaboration. Everyone has unique reasons for building websites. This could be an example. Link.springer.com could have a money-making trick up its sleeve, but it's undetectable for now.

Keywords {πŸ”}

cell, lung, cancer, sclc, expression, mirnas, article, google, scholar, lines, cas, cells, nsclc, mirna, hbecs, shown, expressed, nsclcs, sclcs, microrna, tumor, differentially, groups, levels, micrornas, normal, human, res, small, compared, hbec, relative, center, analysis, pathogenesis, tumors, specific, figure, usa, minna, studies, subtypes, nonsmall, epithelial, diagnostic, carcinoma, results, markers, significantly, croce,

Topics {βœ’οΈ}

egfr-regulated anti-apoptotic factor small-cell lung carcinoma small-cell lung cancer small-cell lung cancer small noncoding rnas small cell carcinoma p16/cyclin d1/rb pathway utsw/mdacc lung spore genome-wide expression patterns cancer invasion-metastasis cascade 5'-phosphate-cytidyl-uridyl-cy3-3' uncovering growth-suppressive micrornas squamous cell carcinoma ]anthrance-induced oral carcinogenesis full size image tailed unpaired t-test increased tre-binding activity cell line measurement article download pdf multi-dimensional space defined stable blood-based markers false discovery rate therapeutic oncology research cell lines based privacy choices/manage cookies enhances cell proliferation cancer cell lines cancer cell cycles lung cancer preneoplasia explore mirna involvement lung cancer cells great clinical benefit mayo clin proc human lung cancers normal lung tissues exp lung res normal lung cells airway epithelial progenitors lung cancer subtypes tumor cell populations authors’ original file human lung tumors small cell small-cell tumor suppressor genes lung stem cells primary tissue specimens multi-dimensional space microrna-based approach cell line

Questions {❓}

  • Gazdar AF, Gao B, Minna JD: Lung cancer cell lines: Useless artifacts or invaluable tools for medical science?
  • Giangreco A, Groot KR, Janes SM: Lung cancer and lung stem cells: strange bedfellows?
  • Puglisi M, Dolly S, Faria A, Myerson JS, Popat S, O'Brien ME: Treatment options for small cell lung cancer - do we have more choice?

Schema {πŸ—ΊοΈ}

WebPage:
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         headline:MicroRNA expression distinguishes SCLC from NSCLC lung tumor cells and suggests a possible pathological relationship between SCLCs and NSCLCs
         description:Recent studies have shown that microRNAs (miRNAs) play roles in tumorigenesis and are reliable classifiers of certain cancer types and subtypes. However, the role of miRNAs in the pathogenesis and diagnosis of small cell carcinoma (SCLC), the majority of which represent the most aggressive lung tumors, has not been investigated. In order to explore miRNA involvement in the pathogenesis of small cell lung carcinoma (SCLC) and the potential role of miRNAs in SCLC diagnosis, we compared the miRNA expression profile of a set of SCLC cell lines to that of a set of non-small cell lung cancer (NSCLC) cell lines and normal immortalized human bronchial epithelial cells (HBECs) using microarray analysis. Our results show that miRNA profiles reliably distinguish SCLC cell lines from NSCLC and HBEC cell lines. Further analysis of the miRNA expression profile of the two subtypes of lung cancer cell lines indicates that the expression levels of the majority of the miRNAs that are differentially expressed in SCLC cells relative to NSCLC cells and HBECs show a progressive trend from HBECs to NSCLC cells to SCLC cells. The distinctive miRNA expression signature of SCLCs relative to NSCLCs and HBECs suggests that miRNA profiles have the potential to serve as a diagnostic marker of SCLC lung tumors. The progressive trend of miRNA profile changes from HBECs to NSCLCs to SCLCs suggests a possible pathological relationship between SCLCs and NSCLCs, and suggests that the increasing dysregulation of miRNA expression may play a role in lung tumor progression. The specific role of these miRNAs in lung tumor pathogenesis and differentiation need to be investigated further in future studies.
         datePublished:2010-06-17T00:00:00Z
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            miRNA Expression
            Adenomatous Polyposis Coli
            NSCLC Cell
            Lung Cancer Cell Line
            Small Cell Lung Carcinoma
            Cancer Research
            Immunology
            Apoptosis
            Oncology
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      headline:MicroRNA expression distinguishes SCLC from NSCLC lung tumor cells and suggests a possible pathological relationship between SCLCs and NSCLCs
      description:Recent studies have shown that microRNAs (miRNAs) play roles in tumorigenesis and are reliable classifiers of certain cancer types and subtypes. However, the role of miRNAs in the pathogenesis and diagnosis of small cell carcinoma (SCLC), the majority of which represent the most aggressive lung tumors, has not been investigated. In order to explore miRNA involvement in the pathogenesis of small cell lung carcinoma (SCLC) and the potential role of miRNAs in SCLC diagnosis, we compared the miRNA expression profile of a set of SCLC cell lines to that of a set of non-small cell lung cancer (NSCLC) cell lines and normal immortalized human bronchial epithelial cells (HBECs) using microarray analysis. Our results show that miRNA profiles reliably distinguish SCLC cell lines from NSCLC and HBEC cell lines. Further analysis of the miRNA expression profile of the two subtypes of lung cancer cell lines indicates that the expression levels of the majority of the miRNAs that are differentially expressed in SCLC cells relative to NSCLC cells and HBECs show a progressive trend from HBECs to NSCLC cells to SCLC cells. The distinctive miRNA expression signature of SCLCs relative to NSCLCs and HBECs suggests that miRNA profiles have the potential to serve as a diagnostic marker of SCLC lung tumors. The progressive trend of miRNA profile changes from HBECs to NSCLCs to SCLCs suggests a possible pathological relationship between SCLCs and NSCLCs, and suggests that the increasing dysregulation of miRNA expression may play a role in lung tumor progression. The specific role of these miRNAs in lung tumor pathogenesis and differentiation need to be investigated further in future studies.
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      dateModified:2010-06-17T00:00:00Z
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         miRNA Expression
         Adenomatous Polyposis Coli
         NSCLC Cell
         Lung Cancer Cell Line
         Small Cell Lung Carcinoma
         Cancer Research
         Immunology
         Apoptosis
         Oncology
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      name:Hamon Center for Therapeutic Oncology Research, UT Southwestern Medical Center, Dallas, USA
      name:Department of Pharmacology, UT Southwestern Medical Center, Dallas, USA
      name:Lineberger Comprehensive Cancer Center, School of Medicine, University of North Carolina School at Chapel Hill, Chapel Hill, USA
      name:Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, USA
      name:Hamon Center for Therapeutic Oncology Research, UT Southwestern Medical Center, Dallas, USA
      name:Department of Pharmacology, UT Southwestern Medical Center, Dallas, USA
      name:Department of Internal Medicine, UT Southwestern Medical Center, Dallas, USA
      name:Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, USA
      name:Hamon Center for Therapeutic Oncology Research, UT Southwestern Medical Center, Dallas, USA
      name:Department of Pathology, UT Southwestern Medical Center, Dallas, USA
      name:Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, USA
      name:McDermott Center for Human Growth and Development, UT Southwestern Medical Center, Dallas, USA
      name:Department of Internal Medicine, UT Southwestern Medical Center, Dallas, USA

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