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Suppression of pancreatic ductal adenocarcinoma growth and metastasis by fibrillar collagens produced selectively by tumor cells
by
Lau, Allison N.
, Carr, Steven A.
, Rickelt, Steffen
, Tian, Chenxi
, Clauser, Karl R.
, Huang, Ying
, Vander Heiden, Matthew G.
, Hynes, Richard O.
in
13/1
/ 13/106
/ 13/109
/ 14/28
/ 14/63
/ 38/77
/ 38/88
/ 38/89
/ 59
/ 631/67/1504/1713
/ 631/67/322
/ 631/67/327
/ 64
/ 64/60
/ 82/51
/ 82/58
/ 82/80
/ 82/83
/ 96
/ Adenocarcinoma
/ Animals
/ Bone morphogenetic protein 1
/ Bone Morphogenetic Protein 1 - metabolism
/ Cancer
/ Carcinoma, Pancreatic Ductal - metabolism
/ Carcinoma, Pancreatic Ductal - pathology
/ Carcinoma, Pancreatic Ductal - secondary
/ Cell Line, Tumor
/ Collagen
/ Collagen (type I)
/ Collagen Type I - chemistry
/ Collagen Type I - genetics
/ Collagen Type I - metabolism
/ Collagen Type I, alpha 1 Chain
/ Data analysis
/ Deposition
/ Disease Progression
/ Drug delivery
/ Extracellular matrix
/ Extracellular Matrix - metabolism
/ Extracellular Matrix Proteins - metabolism
/ Fibrillar Collagens - chemistry
/ Fibrillar Collagens - genetics
/ Fibrillar Collagens - metabolism
/ Humanities and Social Sciences
/ Humans
/ Malignancy
/ Mass spectrometry
/ Mass spectroscopy
/ Metastases
/ Metastasis
/ Mice
/ Mice, Inbred NOD
/ Mice, Knockout
/ Mice, SCID
/ multidisciplinary
/ Mutagenesis
/ Pancreas
/ Pancreatic cancer
/ Pancreatic Neoplasms - genetics
/ Pancreatic Neoplasms - metabolism
/ Pancreatic Neoplasms - pathology
/ Perturbation
/ Procollagen
/ Procollagen - chemistry
/ Procollagen - genetics
/ Procollagen - metabolism
/ Protein Domains
/ Proteinase
/ RNA, Messenger - genetics
/ RNA, Messenger - metabolism
/ Science
/ Science (multidisciplinary)
/ Stromal cells
/ Tumor cells
/ Tumors
2021
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Suppression of pancreatic ductal adenocarcinoma growth and metastasis by fibrillar collagens produced selectively by tumor cells
by
Lau, Allison N.
, Carr, Steven A.
, Rickelt, Steffen
, Tian, Chenxi
, Clauser, Karl R.
, Huang, Ying
, Vander Heiden, Matthew G.
, Hynes, Richard O.
in
13/1
/ 13/106
/ 13/109
/ 14/28
/ 14/63
/ 38/77
/ 38/88
/ 38/89
/ 59
/ 631/67/1504/1713
/ 631/67/322
/ 631/67/327
/ 64
/ 64/60
/ 82/51
/ 82/58
/ 82/80
/ 82/83
/ 96
/ Adenocarcinoma
/ Animals
/ Bone morphogenetic protein 1
/ Bone Morphogenetic Protein 1 - metabolism
/ Cancer
/ Carcinoma, Pancreatic Ductal - metabolism
/ Carcinoma, Pancreatic Ductal - pathology
/ Carcinoma, Pancreatic Ductal - secondary
/ Cell Line, Tumor
/ Collagen
/ Collagen (type I)
/ Collagen Type I - chemistry
/ Collagen Type I - genetics
/ Collagen Type I - metabolism
/ Collagen Type I, alpha 1 Chain
/ Data analysis
/ Deposition
/ Disease Progression
/ Drug delivery
/ Extracellular matrix
/ Extracellular Matrix - metabolism
/ Extracellular Matrix Proteins - metabolism
/ Fibrillar Collagens - chemistry
/ Fibrillar Collagens - genetics
/ Fibrillar Collagens - metabolism
/ Humanities and Social Sciences
/ Humans
/ Malignancy
/ Mass spectrometry
/ Mass spectroscopy
/ Metastases
/ Metastasis
/ Mice
/ Mice, Inbred NOD
/ Mice, Knockout
/ Mice, SCID
/ multidisciplinary
/ Mutagenesis
/ Pancreas
/ Pancreatic cancer
/ Pancreatic Neoplasms - genetics
/ Pancreatic Neoplasms - metabolism
/ Pancreatic Neoplasms - pathology
/ Perturbation
/ Procollagen
/ Procollagen - chemistry
/ Procollagen - genetics
/ Procollagen - metabolism
/ Protein Domains
/ Proteinase
/ RNA, Messenger - genetics
/ RNA, Messenger - metabolism
/ Science
/ Science (multidisciplinary)
/ Stromal cells
/ Tumor cells
/ Tumors
2021
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Suppression of pancreatic ductal adenocarcinoma growth and metastasis by fibrillar collagens produced selectively by tumor cells
by
Lau, Allison N.
, Carr, Steven A.
, Rickelt, Steffen
, Tian, Chenxi
, Clauser, Karl R.
, Huang, Ying
, Vander Heiden, Matthew G.
, Hynes, Richard O.
in
13/1
/ 13/106
/ 13/109
/ 14/28
/ 14/63
/ 38/77
/ 38/88
/ 38/89
/ 59
/ 631/67/1504/1713
/ 631/67/322
/ 631/67/327
/ 64
/ 64/60
/ 82/51
/ 82/58
/ 82/80
/ 82/83
/ 96
/ Adenocarcinoma
/ Animals
/ Bone morphogenetic protein 1
/ Bone Morphogenetic Protein 1 - metabolism
/ Cancer
/ Carcinoma, Pancreatic Ductal - metabolism
/ Carcinoma, Pancreatic Ductal - pathology
/ Carcinoma, Pancreatic Ductal - secondary
/ Cell Line, Tumor
/ Collagen
/ Collagen (type I)
/ Collagen Type I - chemistry
/ Collagen Type I - genetics
/ Collagen Type I - metabolism
/ Collagen Type I, alpha 1 Chain
/ Data analysis
/ Deposition
/ Disease Progression
/ Drug delivery
/ Extracellular matrix
/ Extracellular Matrix - metabolism
/ Extracellular Matrix Proteins - metabolism
/ Fibrillar Collagens - chemistry
/ Fibrillar Collagens - genetics
/ Fibrillar Collagens - metabolism
/ Humanities and Social Sciences
/ Humans
/ Malignancy
/ Mass spectrometry
/ Mass spectroscopy
/ Metastases
/ Metastasis
/ Mice
/ Mice, Inbred NOD
/ Mice, Knockout
/ Mice, SCID
/ multidisciplinary
/ Mutagenesis
/ Pancreas
/ Pancreatic cancer
/ Pancreatic Neoplasms - genetics
/ Pancreatic Neoplasms - metabolism
/ Pancreatic Neoplasms - pathology
/ Perturbation
/ Procollagen
/ Procollagen - chemistry
/ Procollagen - genetics
/ Procollagen - metabolism
/ Protein Domains
/ Proteinase
/ RNA, Messenger - genetics
/ RNA, Messenger - metabolism
/ Science
/ Science (multidisciplinary)
/ Stromal cells
/ Tumor cells
/ Tumors
2021
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Suppression of pancreatic ductal adenocarcinoma growth and metastasis by fibrillar collagens produced selectively by tumor cells
Journal Article
Suppression of pancreatic ductal adenocarcinoma growth and metastasis by fibrillar collagens produced selectively by tumor cells
2021
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Overview
Pancreatic ductal adenocarcinoma (PDAC) has a collagen-rich dense extracellular matrix (ECM) that promotes malignancy of cancer cells and presents a barrier for drug delivery. Data analysis of our published mass spectrometry (MS)-based studies on enriched ECM from samples of progressive PDAC stages reveal that the C-terminal prodomains of fibrillar collagens are partially uncleaved in PDAC ECM, suggesting reduced procollagen C-proteinase activity. We further show that the enzyme responsible for procollagen C-proteinase activity, bone morphogenetic protein1 (BMP1), selectively suppresses tumor growth and metastasis in cells expressing high levels of COL1A1. Although BMP1, as a secreted proteinase, promotes fibrillar collagen deposition from both cancer cells and stromal cells, only cancer-cell-derived procollagen cleavage and deposition suppresses tumor malignancy. These studies reveal a role for cancer-cell-derived fibrillar collagen in selectively restraining tumor growth and suggest stratification of patients based on their tumor epithelial collagen I expression when considering treatments related to perturbation of fibrillar collagens.
Pancreatic ductal adenocarcinoma has a collagen-rich dense extracellular matrix that promotes malignancy of cancer cells. Here, the authors show that fibrillar collagen that is cancer-cell-derived, but not stroma-derived, selectively restrains tumor growth under control of their pC-proteinase, BMP1.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
Subject
/ 13/106
/ 13/109
/ 14/28
/ 14/63
/ 38/77
/ 38/88
/ 38/89
/ 59
/ 64
/ 64/60
/ 82/51
/ 82/58
/ 82/80
/ 82/83
/ 96
/ Animals
/ Bone morphogenetic protein 1
/ Bone Morphogenetic Protein 1 - metabolism
/ Cancer
/ Carcinoma, Pancreatic Ductal - metabolism
/ Carcinoma, Pancreatic Ductal - pathology
/ Carcinoma, Pancreatic Ductal - secondary
/ Collagen
/ Collagen Type I - metabolism
/ Collagen Type I, alpha 1 Chain
/ Extracellular Matrix - metabolism
/ Extracellular Matrix Proteins - metabolism
/ Fibrillar Collagens - chemistry
/ Fibrillar Collagens - genetics
/ Fibrillar Collagens - metabolism
/ Humanities and Social Sciences
/ Humans
/ Mice
/ Pancreas
/ Pancreatic Neoplasms - genetics
/ Pancreatic Neoplasms - metabolism
/ Pancreatic Neoplasms - pathology
/ Science
/ Tumors
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