Clinical End-Points Associated with Mycobacterium tuberculosis and Lung Cancer: Implications into Host-Pathogen Interaction and Coevolution.

There is a recent emerging theory that suggests a cross-link between pathogens and cancer. In this context, we examined the association between the Mycobacterium tuberculosis (MTB) with its L-forms (MTB-L) and lung cancer. In the present study, we have optimized and applied a highly sensitive assay...

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Publicado en:BioMed Research International Vol. 2015; pp. 1 - 10
Autores principales: Yansheng Tian, Tong Hao, Bin Cao, Wei Zhang, Yan Ma, Qiang Lin, Xiaomin Li
Formato: pictorial research tables/charts Journal Article
Publicado: Wiley-Blackwell 10/25/2015
Acceso en línea:Ver este registro en EBSCOhost
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      dt: 10/25/2015
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      pub: Wiley-Blackwell
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        10.1155/2015/827829
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        atl: Clinical End-Points Associated with Mycobacterium tuberculosis and Lung Cancer: Implications into Host-Pathogen Interaction and Coevolution.
      aug:
        au:
          Yansheng Tian
          Tong Hao
          Bin Cao
          Wei Zhang
          Yan Ma
          Qiang Lin
          Xiaomin Li
        affil: Central Laboratory, North China Oilfield Hospital of Hebei Medical University, Renqiu, Hebei 062552, China
      sug:
        subj:
          Mycobacterium Tuberculosis
          Lung Neoplasms Microbiology
          Microbiologic Phenomena
          Evolution
          Human
          Biological Assay
          Confounding Variable
          Linear Regression
      ab: There is a recent emerging theory that suggests a cross-link between pathogens and cancer. In this context, we examined the association between the Mycobacterium tuberculosis (MTB) with its L-forms (MTB-L) and lung cancer. In the present study, we have optimized and applied a highly sensitive assay to detect the presence of MTB and MTB-L in 187 lung cancer samples and 39 samples of other cancer origins. By carefully controlling confounding factors, we have found that 62% of the lung cancer samples are MTB-L positive, while only 5.1% of the other cancer samples are MTB-L positive. Through generalized linear models and random forest models, we have further identified a set of clinical end-points that are strongly associated with MTB-L presence. Our finding provides the basis for future studies to investigate the underlying mechanism linking MTB-L infection to lung cancer development.
      pubtype: Academic Journal
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        pictorial
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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