Apoptosis research paper

The elucidation of the apoptosis pathway in C. Intracellularly, however, these members contain an area of weak homology required to transduce a cell death signal which was termed the death domain DD. PDF Abstract Apoptosis, also called programmed cell death, has attracted great attention in recent years.

Michael Hengartner also identified a gene with an opposite effect: Curriecoined the term "apoptosis" in order to differentiate naturally occurring developmental cell death, from the necrosis that results from acute tissue injury.

Apoptosis in cancer: from pathogenesis to treatment

Ptosis means to fall. First, studies with the small nematode Caenorhabditis elegans have identified a number of apoptosis regulating genes—the first evidence that cell death is an active process under genetic control.

The first of three recent breakthroughs in apoptosis research comes from the genetic study of genes that control apoptotic cell death in the nematode Caenorhabditis elegans. The conservation in both sequence and function between nematode and mammalian cell death genes indicates that apoptosis is of ancient evolutionary origin, and it suggests that worms and humans use similar conserved mechanisms to get rid of cells.

Apoptosis - Research Paper Example

Caspases are central to the mechanism of apoptosis as they are both the initiators and executioners. Later, there is internucleosomal cleavage of DNA into oligonucleosomes in multiples of to base pairs by endonucleases.

History of apoptosis research

Both pathways eventually lead to a common pathway or the execution phase of apoptosis. There are three pathways by which caspases can be activated. Caspase-8 is activated by binding to the DISC 5. Activated caspases cleave many vital cellular proteins and break up the nuclear scaffold and cytoskeleton.

The pronunciation "a POP tuh sis", although commonly used, ignores the origin of the word. Apo means away, off or apart.

The plasma membrane is intact throughout the total process. Some genes, such as ces-1 and ces-2, function only in a small number of cells and affect the decision of individual cells to activate the death program.

Although there have been scattered reports on the topic of cell death for more than a century, the 20, publications on this topic within the past 5 years reflect a shift from historically mild interest to contemporary fascination [12].

Advances in apoptosis research

In the worm three genes—ced-3, ced-4, and ced-9—are directly involved in controlling the execution of apoptosis during development 1. Another specific feature of apoptosis is the activation of a group of enzymes belonging to Apoptosis research paper cysteine protease family named caspases.

The second breakthrough is related to the discovery of a family of receptors that can specifically trigger apoptosis. Only some of them, however, have been detected as part of an in vivo complex with their receptors formed in a ligand-dependent fashion.

Although the biochemical changes explain in part some of the morphological changes in apoptosis, it is important to note that biochemical analyses of DNA fragmentation or caspase activation should not be used to define apoptosis, as apoptosis can occur without oligonucleosomal DNA fragmentation and can be caspase-independent [ 21 ].

This is followed by a characteristic breakdown of DNA into large 50 to kilobase pieces [ 18 ]. Apaf-1, a recently identified CED-4 homolog, is similarly required for the processing of caspase-3 in mammalian cells 2.

Key components of the apoptosis machinery seem to be conserved between humans and nematodes. A third less well-known initiation pathway is the intrinsic endoplasmic reticulum pathway [ 22 ]. It was at this lab that during the s and s, a team led by John Sulston succeeded in tracing the nematode Caenorhabditis elegans entire embryonic cell lineage.

The ces-2 gene has recently been shown to encode a homolog of the human oncogene Hlf hepatic leukemia factor 3. DD-containing molecules are specialized adapter molecules coupling to the apoptosis executioners, which are in many instances members of the caspase family of proteases. If the remnants of apoptotic cells are not phagocytosed such as in the case of an artificial cell culture environment, they will undergo degradation that resembles necrosis and the condition is termed secondary necrosis [ 13 ].The Role of Apoptosis in Cancer Therapy activate effector caspases or amplify the caspase cascades by increased activation of initiator caspases,13 Then the effector caspases cleave intracellular substrates, culminating in cell death,14Bcl-2 family members of proapoptotic and antiapoptotic proteins regulate.

Sep 26,  · Apoptosis in cancer: from pathogenesis to treatment. Rebecca SY Wong 1 Apoptosis is an ordered and orchestrated cellular process that occurs in physiological and pathological conditions.

It is also one of the most studied topics among cell biologists. it remains one of the most investigated processes in biologic research. The paper "Apoptosis " describes that apoptosis is an important programmed cell death process which exists and occurs in multicellular organisms.

It is. Ever since apoptosis was described by Kerr et al in the 's, it remains one of the most investigated processes in biologic research. Being a highly selective process, apoptosis is important in both physiological and pathological conditions [ 9, 10 ].

InMichael Hengartner published a paper showing that ced-9 had similar sequence to bcl Ina protein similar to CED-4 was identified and named Apaf-1 (apoptotic protease activating factor). "History of Apoptosis Research". eLS. doi. have shown that moderate autophagy has a protective effect against apoptosis in NP cells.

Berberine (BBR) is an alkaloid compound .

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Apoptosis research paper
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