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Expression ratio of the TGFβ-inducible gene MYO10 is prognostic for overall survival of squamous cell lung cancer patients and predicts chemotherapy response
by
Herth, F. J.
, Titkova, I.
, Dienemann, H.
, Schneider, M. A.
, Rosenblatt, M.
, Thomas, M.
, Warth, A.
, Busch, H.
, Dvornikov, D.
, Klingmüller, U.
, Muley, T.
, Schilling, M.
, Szczygieł, M.
, Boerries, M.
, Meister, M.
, Ohse, S.
, Timmer, J.
in
13/109
/ 13/2
/ 13/89
/ 14/63
/ 45/91
/ 631/67/1612/1350
/ 631/80/86/2368
/ 692/4028/67/1612/1350
/ 692/53/2422
/ 692/53/2423
/ 96/21
/ 96/95
/ Actin
/ Carcinogenesis
/ Carcinoma, Squamous Cell - diagnosis
/ Carcinoma, Squamous Cell - drug therapy
/ Carcinoma, Squamous Cell - genetics
/ Carcinoma, Squamous Cell - pathology
/ Cell Line, Tumor
/ Cell survival
/ Chemotherapy
/ Collagen
/ Cytoskeleton
/ Deregulation
/ Gene expression
/ Gene Expression Regulation, Neoplastic
/ Genomes
/ Humanities and Social Sciences
/ Humans
/ Invasiveness
/ Lung cancer
/ Lung carcinoma
/ Lung Neoplasms - diagnosis
/ Lung Neoplasms - drug therapy
/ Lung Neoplasms - genetics
/ Lung Neoplasms - pathology
/ Motility
/ multidisciplinary
/ Myosin
/ Myosins - genetics
/ Neoplasm Invasiveness
/ Phenotypes
/ Prognosis
/ RNA, Messenger - genetics
/ RNA, Messenger - metabolism
/ Science
/ Science (multidisciplinary)
/ Squamous cell carcinoma
/ Survival Analysis
/ Therapeutic applications
/ Transcriptional Activation - drug effects
/ Transforming Growth Factor beta - pharmacology
/ Transforming growth factor-b
2018
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Expression ratio of the TGFβ-inducible gene MYO10 is prognostic for overall survival of squamous cell lung cancer patients and predicts chemotherapy response
by
Herth, F. J.
, Titkova, I.
, Dienemann, H.
, Schneider, M. A.
, Rosenblatt, M.
, Thomas, M.
, Warth, A.
, Busch, H.
, Dvornikov, D.
, Klingmüller, U.
, Muley, T.
, Schilling, M.
, Szczygieł, M.
, Boerries, M.
, Meister, M.
, Ohse, S.
, Timmer, J.
in
13/109
/ 13/2
/ 13/89
/ 14/63
/ 45/91
/ 631/67/1612/1350
/ 631/80/86/2368
/ 692/4028/67/1612/1350
/ 692/53/2422
/ 692/53/2423
/ 96/21
/ 96/95
/ Actin
/ Carcinogenesis
/ Carcinoma, Squamous Cell - diagnosis
/ Carcinoma, Squamous Cell - drug therapy
/ Carcinoma, Squamous Cell - genetics
/ Carcinoma, Squamous Cell - pathology
/ Cell Line, Tumor
/ Cell survival
/ Chemotherapy
/ Collagen
/ Cytoskeleton
/ Deregulation
/ Gene expression
/ Gene Expression Regulation, Neoplastic
/ Genomes
/ Humanities and Social Sciences
/ Humans
/ Invasiveness
/ Lung cancer
/ Lung carcinoma
/ Lung Neoplasms - diagnosis
/ Lung Neoplasms - drug therapy
/ Lung Neoplasms - genetics
/ Lung Neoplasms - pathology
/ Motility
/ multidisciplinary
/ Myosin
/ Myosins - genetics
/ Neoplasm Invasiveness
/ Phenotypes
/ Prognosis
/ RNA, Messenger - genetics
/ RNA, Messenger - metabolism
/ Science
/ Science (multidisciplinary)
/ Squamous cell carcinoma
/ Survival Analysis
/ Therapeutic applications
/ Transcriptional Activation - drug effects
/ Transforming Growth Factor beta - pharmacology
/ Transforming growth factor-b
2018
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Expression ratio of the TGFβ-inducible gene MYO10 is prognostic for overall survival of squamous cell lung cancer patients and predicts chemotherapy response
by
Herth, F. J.
, Titkova, I.
, Dienemann, H.
, Schneider, M. A.
, Rosenblatt, M.
, Thomas, M.
, Warth, A.
, Busch, H.
, Dvornikov, D.
, Klingmüller, U.
, Muley, T.
, Schilling, M.
, Szczygieł, M.
, Boerries, M.
, Meister, M.
, Ohse, S.
, Timmer, J.
in
13/109
/ 13/2
/ 13/89
/ 14/63
/ 45/91
/ 631/67/1612/1350
/ 631/80/86/2368
/ 692/4028/67/1612/1350
/ 692/53/2422
/ 692/53/2423
/ 96/21
/ 96/95
/ Actin
/ Carcinogenesis
/ Carcinoma, Squamous Cell - diagnosis
/ Carcinoma, Squamous Cell - drug therapy
/ Carcinoma, Squamous Cell - genetics
/ Carcinoma, Squamous Cell - pathology
/ Cell Line, Tumor
/ Cell survival
/ Chemotherapy
/ Collagen
/ Cytoskeleton
/ Deregulation
/ Gene expression
/ Gene Expression Regulation, Neoplastic
/ Genomes
/ Humanities and Social Sciences
/ Humans
/ Invasiveness
/ Lung cancer
/ Lung carcinoma
/ Lung Neoplasms - diagnosis
/ Lung Neoplasms - drug therapy
/ Lung Neoplasms - genetics
/ Lung Neoplasms - pathology
/ Motility
/ multidisciplinary
/ Myosin
/ Myosins - genetics
/ Neoplasm Invasiveness
/ Phenotypes
/ Prognosis
/ RNA, Messenger - genetics
/ RNA, Messenger - metabolism
/ Science
/ Science (multidisciplinary)
/ Squamous cell carcinoma
/ Survival Analysis
/ Therapeutic applications
/ Transcriptional Activation - drug effects
/ Transforming Growth Factor beta - pharmacology
/ Transforming growth factor-b
2018
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Expression ratio of the TGFβ-inducible gene MYO10 is prognostic for overall survival of squamous cell lung cancer patients and predicts chemotherapy response
Journal Article
Expression ratio of the TGFβ-inducible gene MYO10 is prognostic for overall survival of squamous cell lung cancer patients and predicts chemotherapy response
2018
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Overview
In lung cancer a deregulation of Transforming Growth Factor-β (TGFβ) signaling has been observed. Yet, the impact of TGFβ in squamous cell carcinoma of the lung (LUSC) remained to be determined. We combined phenotypic and transcriptome-wide studies and showed that the stimulation of the LUSC cell line SK-MES1 with TGFβ results in an increase of migratory invasive properties. The analysis of the dynamics of gene expression by next-generation sequencing revealed that TGFβ stimulation orchestrates the upregulation of numerous motility- and actin cytoskeleton-related genes. Among these the non-muscle myosin 10 (
MYO10
) showed the highest upregulation in a LUSC patient cohort of the Cancer Genome Atlas (TCGA). Knockdown of
MYO10
abrogated TGFβ-induced collagen gel invasion of SK-MES1 cells. The analysis of
MYO10
mRNA expression in paired tissues of 151 LUSC patients with corresponding 80-month clinical follow-up data showed that the mRNA expression ratio of
MYO10
in tumor and tumor-free tissue is prognostic for overall survival of LUSC patients and predictive for the response of these patients to adjuvant chemotherapy. Thus,
MYO10
represents a new clinical biomarker for this aggressive disease and due to its role in cellular motility and invasion could serve as a potential molecular target for therapeutic interventions in patients with LUSC.
Publisher
Nature Publishing Group UK,Nature Publishing Group
Subject
/ 13/2
/ 13/89
/ 14/63
/ 45/91
/ 96/21
/ 96/95
/ Actin
/ Carcinoma, Squamous Cell - diagnosis
/ Carcinoma, Squamous Cell - drug therapy
/ Carcinoma, Squamous Cell - genetics
/ Carcinoma, Squamous Cell - pathology
/ Collagen
/ Gene Expression Regulation, Neoplastic
/ Genomes
/ Humanities and Social Sciences
/ Humans
/ Lung Neoplasms - drug therapy
/ Motility
/ Myosin
/ Science
/ Transcriptional Activation - drug effects
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