Target Name: TP53AIP1
NCBI ID: G63970
Review Report on TP53AIP1 Target / Biomarker Content of Review Report on TP53AIP1 Target / Biomarker
TP53AIP1
Other Name(s): P53-regulated apoptosis-inducing protein 1 (isoform a) | Tumor protein p53 regulated apoptosis inducing protein 1, transcript variant 1 | P53AIP1 | TP53AIP1 variant 1 | TPIP1_HUMAN | tumor protein p53 regulated apoptosis inducing protein 1 | p53-regulated apoptosis-inducing protein 1 | p53AIP1

TP53AIP1: A Potential Drug Target and Biomarker for Apoptosis

Introduction

Apoptosis, the programmed cell death, is a crucial aspect of various biological processes, including development, growth, and maintenance of tissue homeostasis. The regulation of apoptosis is critical for the survival of cells and organisms. The tumor suppressor protein TP53 is one of the key transcription factors that regulates apoptosis. TP53AIP1, a splice variant of the tumor suppressor protein TP53, has been shown to play a crucial role in regulating apoptosis. In this article, we will discuss the potential implications of TP53AIP1 as a drug target and biomarker.

Structure and Function

The tumor suppressor protein TP53 is a 180-kDa protein that is highly conserved across various species. It is composed of a N-terminal domain, a transmembrane domain, and a C-terminal domain. The C-terminal domain contains the critical regulatory element , the TP53 gene transcription factor domain, which is responsible for binding to DNA and regulating apoptosis.

The TP53 gene is located on chromosome 17 and has four splice variants, isoform A, isoform B, isoform C, and isoform D. Isoform A is the most abundant and well-studied isoform, and it is the only isoform that functions in cell cycle regulation.

The TP53AIP1 gene was identified as a potential drug target and biomarker for apoptosis. The AIP1 gene is located on chromosome 16 and encodes a protein that is similar to TP53AIP1. The AIP1 protein has been shown to play a critical role in regulating apoptosis in various cellular processes, including cell cycle progression, DNA damage repair, and cell survival.

Expression and Regulation

TP53AIP1 is expressed in various tissues and cells, including cancer cells, and has been shown to be involved in the regulation of apoptosis. The expression of TP53AIP1 is regulated by various factors, including DNA damage, cellular stress, and hormonal changes [ 8].

The regulation of TP53AIP1 expression is complex and involves multiple mechanisms. One of the known mechanisms involves the interaction between TP53AIP1 and the transcription factor p21 (transforming growth factor-beta 1). This interaction results in the recruitment of p21 to the TP53AIP1 gene and the inhibition of its nuclear translocation.

The other known mechanism involves the regulation of TP53AIP1 expression by the microRNA (miRNA) pathway. miRNAs are a class of short RNA molecules that can influence gene expression. It has been found that miRNA can regulate the expression of TP53AIP1, and TP53AIP1 can also regulate the stability of miRNA through miRNA.

Drug Targeting and Biomarkers

The regulation of apoptosis by TP53AIP1 is a promising target for drug development. The inhibition of TP53AIP1 has been shown to promote apoptosis in various cellular processes, including cancer growth and chemotherapy resistance.

In addition to its potential as a drug target, TP53AIP1 has also been shown to be a potential biomarker for apoptosis. The levels of TP53AIP1 have been shown to be elevated in various cellular processes, including apoptosis, in response to stress, such as chemotherapy or radiation. Therefore, TP53AIP1 can be used as a biomarker for

Protein Name: Tumor Protein P53 Regulated Apoptosis Inducing Protein 1

Functions: May play an important role in mediating p53/TP53-dependent apoptosis

The "TP53AIP1 Target / Biomarker Review Report" is a customizable review of hundreds up to thousends of related scientific research literature by AI technology, covering specific information about TP53AIP1 comprehensively, including but not limited to:
•   general information;
•   protein structure and compound binding;
•   protein biological mechanisms;
•   its importance;
•   the target screening and validation;
•   expression level;
•   disease relevance;
•   drug resistance;
•   related combination drugs;
•   pharmacochemistry experiments;
•   related patent analysis;
•   advantages and risks of development, etc.
The report is helpful for project application, drug molecule design, research progress updates, publication of research papers, patent applications, etc. If you are interested to get a full version of this report, please feel free to contact us at BD@silexon.ai

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