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Matrix metalloproteinase and its drug targets therapy in solid and hematological malignancies: an overview.

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TLDR
Exploration and exploitation of MMP and TIMP balance in various malignant and nonmalignant lesions is going to be one of the most interesting facets of future use of this system for human health care.
Abstract
Matrix metalloproteinase (MMP) comprises a family of zinc-dependent endopeptidases that degrade various components of the extracellular matrix (ECM) and basement membrane. MMPs are involved in solid and hematological malignancy through modification of cell growth, activation of cancer cells and modulation of immune functions. Several polymorphisms of different MMPs such as MMP-1 (-1607 1G/2G), MMP-2 (-1306 C/T), MMP-3 (-1171 5A/6A) & MMP-9 (-1562 C/T) and their expression levels have been well documented in different types of solid cancer. These polymorphic variations were found to be associated with angiogenesis, cancer progression, invasion and metastasis. There is paucity of data available in the field of hematological malignancies. Hence the field of matrix biology of hematological malignancies is an area of active exploration. A number of MMP inhibitors (MMPIs) have been developed for the cancer treatment. The most extensively studied classes of MMP inhibitors include Batimastat, Marismastat, Salimatat, Prinomastat and Tanomastat. However, their efficacy and action have not been confirmed and more data is required. The application of one or more selective targeted MMPIs in combination with conventional anti-leukemic treatment may represent a positive approach in combat against hematopoietic malignancies. Balance of MMPs and TIMPs is altered in different malignancies and biochemical pathways. These alternations will add another dimension in the matrix biology of both solid tumor and leukemia. MMP and TIMP singly and in combination are increasingly being recognized as an important player in basic cellular biology. Exploration and exploitation of MMP and TIMP balance in various malignant and nonmalignant lesions is going to be one of the most interesting facets of future use of this system for human health care.

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Journal ArticleDOI

Matrix Metalloproteinases: A challenging paradigm of cancer management

TL;DR: The regulatory role of MMPs in cancer progression, current strategies in targeting MMP's for cancer treatment including prodrug design and tumor imaging, and therapeutic value of M MPs as biomarkers in breast, lung, and prostate cancers are discussed.
Journal ArticleDOI

Matrix metalloproteinases: their functional role in lung cancer.

TL;DR: This review has summarized and critically reviewed the published works on the role of MMPs in non-small-cell lung cancer, their various types and roles in lung cancer metastasis including invasion, migration and angiogenesis.
Journal ArticleDOI

Matrix metalloproteinase 13-containing exosomes promote nasopharyngeal carcinoma metastasis

TL;DR: It is found that MMP13 was overexpressed in NPC cells and exosomes purified from conditioned medium as well as NPC patients’ plasma and transwell analysis revealed that M MP13‐containing exosome facilitated the metastasis of NPC cells.
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Intricate functions of matrix metalloproteinases in physiological and pathological conditions

TL;DR: A review article summarized the recent advances in understanding the role of MMPs in physiological and pathological conditions and suggested drugs specifically targeting individual M MPs could revolutionize the treatment of a great number of health conditions and tremendously reduce their burden.
Journal ArticleDOI

Cell–matrix interactions: focus on proteoglycan–proteinase interplay and pharmacological targeting in cancer

TL;DR: The emerging biological roles of proteoglycans and proteinases are described, with a special emphasis on their complex interplay, and future challenges with respect to targeting this axis in the treatment of cancer are discussed.
References
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Journal ArticleDOI

Matrix metalloproteinases and tissue inhibitors of metalloproteinases: structure, function, and biochemistry.

TL;DR: This review describes the members of the matrixin family and discusses substrate specificity, domain structure and function, the activation of proMMPs, the regulation of matrixin activity by tissue inhibitors of metalloproteinases, and their pathophysiological implication.
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How Matrix Metalloproteinases Regulate Cell Behavior

TL;DR: Recent advances shed light on how the structure and function of the MMPs are related and on how their transcription, secretion, activation, inhibition, localization, and clearance are controlled.
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Matrix metalloproteinase-9 triggers the angiogenic switch during carcinogenesis

TL;DR: The results show that MMP-9 is a component of theAngiogenic switch, and MMP inhibitors reduce angiogenic switching, and tumour number and growth, as does genetic ablation of M MP-9.
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A matrix metalloproteinase expressed on the surface of invasive tumour cells

TL;DR: The cloning of the complemen-tary DNA encoding a new matrix metalloproteinase with a potential transmembrane domain is reported, which may trigger invasion by tumour cells by activating pro-gelatinase A on the tumour cell surface.
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MMP-9/Gelatinase B Is a Key Regulator of Growth Plate Angiogenesis and Apoptosis of Hypertrophic Chondrocytes

TL;DR: Transplantation of wild-type bone marrow cells rescues vascularization and ossification in gelatinase B-null growth plates, indicating that these processes are mediated by gelatinaseB-expressing cells of bone marrow origin, designated chondroclasts.
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