Javascript must be enabled to continue!
Apoptosis and its clinical impact
View through CrossRef
AbstractBackgroundApoptosis or programmed cell death is an orderly cascade that can be regulated and ultimately results in the demise of the cell. Induction of apoptosis can occur by various chemical and biologic agents. Initiation of apoptosis leads to activation of effector molecules particularly caspases. These proteases cleave distinct protein substrates, resulting in the morphologic changes seen in apoptosis. This form of cell death is involved in almost every physiologic and pathogenic process in the body. For this reason the ability to control apoptosis has important therapeutic ramifications.ResultsThis article reviews the history of the investigation of apoptosis and summarizes the most important pathways and regulatory molecules involved in this process. The major regulators of apoptosis, including the Bcl‐2, caspase, and inhibitor of apoptosis families, are examined. The two major apoptotic pathways, including the extrinsic/cell surface death receptor and the intrinsic/mitochondrial pathways, are discussed. A major emphasis is given to examining the relationship between apoptosis and certain disease processes. This review specifically focuses on the importance of apoptosis research in the development of new methods of management of cancer with an emphasis in head and neck oncology.ConclusionsApoptosis is a rapidly growing field. The understanding of the mechanisms and effector molecules controlling this form of cell death is evolving. On the basis of increasing knowledge of how programmed cell death is regulated and the improvements in designing and developing gene therapies and chemicals that are more accurate in targeting specific molecules, the control of apoptosis will become more important in the clinical setting. This possibility will open the door for new therapeutic endeavors in many areas of medicine and specifically in the area of oncology. © 2001 John Wiley & Sons, Inc. Head Neck 23: 409–425, 2001.
Title: Apoptosis and its clinical impact
Description:
AbstractBackgroundApoptosis or programmed cell death is an orderly cascade that can be regulated and ultimately results in the demise of the cell.
Induction of apoptosis can occur by various chemical and biologic agents.
Initiation of apoptosis leads to activation of effector molecules particularly caspases.
These proteases cleave distinct protein substrates, resulting in the morphologic changes seen in apoptosis.
This form of cell death is involved in almost every physiologic and pathogenic process in the body.
For this reason the ability to control apoptosis has important therapeutic ramifications.
ResultsThis article reviews the history of the investigation of apoptosis and summarizes the most important pathways and regulatory molecules involved in this process.
The major regulators of apoptosis, including the Bcl‐2, caspase, and inhibitor of apoptosis families, are examined.
The two major apoptotic pathways, including the extrinsic/cell surface death receptor and the intrinsic/mitochondrial pathways, are discussed.
A major emphasis is given to examining the relationship between apoptosis and certain disease processes.
This review specifically focuses on the importance of apoptosis research in the development of new methods of management of cancer with an emphasis in head and neck oncology.
ConclusionsApoptosis is a rapidly growing field.
The understanding of the mechanisms and effector molecules controlling this form of cell death is evolving.
On the basis of increasing knowledge of how programmed cell death is regulated and the improvements in designing and developing gene therapies and chemicals that are more accurate in targeting specific molecules, the control of apoptosis will become more important in the clinical setting.
This possibility will open the door for new therapeutic endeavors in many areas of medicine and specifically in the area of oncology.
© 2001 John Wiley & Sons, Inc.
Head Neck 23: 409–425, 2001.
Related Results
V-ATPase Deficiency Aggravates Hypoxia-induced Spermatogenesis Reduction by Promoting Spermatocyte Apoptosis via the JNK/c-Jun Pathway in Mice
V-ATPase Deficiency Aggravates Hypoxia-induced Spermatogenesis Reduction by Promoting Spermatocyte Apoptosis via the JNK/c-Jun Pathway in Mice
Abstract
Spermatocyte apoptosis is the primary cause of poor outcome after hypoxia-triggered spermatogenesis reduction (HSR). The vacuolar H+-ATPase (V-ATPase) has been fou...
Molecular Mechanism Analysis the Apoptosis of Leukemia Cells Induced By CRM1 Selective Inhibitor KPT-330
Molecular Mechanism Analysis the Apoptosis of Leukemia Cells Induced By CRM1 Selective Inhibitor KPT-330
Abstract
Objective: To investigate the effect and mechanisms of KPT-330 on cell apoptosis of human leukemia cells. Methods: CCK-8 assay was used to quantify the grow...
The C. elegans TIA‐1/TIAR homolog TIAR‐1 is required to induce germ cell apoptosis
The C. elegans TIA‐1/TIAR homolog TIAR‐1 is required to induce germ cell apoptosis
SummaryIn Caenorhabditis elegans, physiological germ cell apoptosis eliminates more than half of the cells in the hermaphrodite gonad to support gamete quality and germline homeost...
Lymphocytes Apoptosis in Patients with Acute Exacerbation of Asthma
Lymphocytes Apoptosis in Patients with Acute Exacerbation of Asthma
Asthma is characterized by airway inflammation, which can be now assessed by the analysis of induced sputum . Ten patients with asthma were investigated during acute exacerbation f...
ANTP-SmacN7 Enhances Radiosensitivity in TPC-1 Cells Through XIAP-Mediated Activation of Apoptotic Protein
ANTP-SmacN7 Enhances Radiosensitivity in TPC-1 Cells Through XIAP-Mediated Activation of Apoptotic Protein
Abstract
Objective: A subset of differentiated thyroid cancer still lacks effective treatment options, such as locally advanced or metastatic patients. Some of these patien...
Functional heterogeneity of anti-endothelial cell antibodies
Functional heterogeneity of anti-endothelial cell antibodies
SUMMARYWhile it has been claimed that some anti-endothelial cell antibodies (AECA) activate EC, there is also evidence that others trigger apoptosis. To address the issue of whethe...
ROLE OF HMGB1 IN DOXORUBICIN-INDUCED MYOCARDIAL APOPTOSIS AND ITS REGULATION PATHWAY
ROLE OF HMGB1 IN DOXORUBICIN-INDUCED MYOCARDIAL APOPTOSIS AND ITS REGULATION PATHWAY
Objectives
Doxorubicin (DOX) is a widely used anti-tumour agent. The clinical application of the medication is limited by its side effect which can elicit myocard...
Up-regulated macrophage migration inhibitory factor protects apoptosis of dermal fibroblasts in patients with systemic sclerosis
Up-regulated macrophage migration inhibitory factor protects apoptosis of dermal fibroblasts in patients with systemic sclerosis
Summary
Macrophage migration inhibitory factor (MIF) is a proinflammatory cytokine that has been demonstrated to regulate the apoptosis of several cell types. Dysreg...

