Target Name: NIBAN2
NCBI ID: G64855
Review Report on NIBAN2 Target / Biomarker Content of Review Report on NIBAN2 Target / Biomarker
NIBAN2
Other Name(s): melanoma invasion by ERK | MINERVA | FAM129B | MEG-3 | Protein FAM129B | bA356B19.6 | NIBAN2 variant 1 | BA356B19.6 | FLJ22298 | Niban apoptosis regulator 2, transcript variant 1 | Meg-3 | OC58 | FLJ13518 | family with sequence similarity 129 member B | niban-like protein 1 | Melanoma invasion by ERK | Protein Niban 2 | niban apoptosis regulator 2 | NIBA2_HUMAN | FLJ22151 | Protein Niban 2 (isoform 1) | C9orf88 | DKFZP434H0820

NIBAN2: A Potential Drug Target and Biomarker for Melanoma Invasion by ERK

Melanoma is one of the most aggressive forms of skin cancer, with a high incidence rate and a poor prognosis. Despite advances in surgical and radiation treatments, the survival rate for melanoma remains poor, and the disease is often lethal. Therefore, there is a need for new treatments and biomarkers to improve outcomes.

NIBAN2, a nuclear protein that is expressed in various tissues and cell types, including melanoma, has been identified as a potential drug target and biomarker for melanoma invasion by ERK (Erk-associated protein kinase). In this article, we will discuss the biology of ERK, its role in melanoma progression, and the potential implications of targeting NIBAN2 for melanoma treatment.

The ERK pathway is a well-established signaling pathway that regulates various cellular processes, including cell growth, differentiation, and survival. ERK is a protein that is involved in the catalytic process of the catalytic domain, which plays a crucial role in the regulation of cell growth and the maintenance of cellular homeostasis.

Melanoma is a type of skin cancer that is characterized by the melanocytes, which are the pigment-producing cells in the skin. Melanoma can arise from various stages of skin development, including melanocytes, melanoma-infiltrating cells, or squamous cell carcinoma. Despite advances in surgical and radiation treatments, the survival rate for melanoma remains poor, with a 5-year survival rate of only around 15%.

ERK has been implicated in melanoma progression and tumor growth. Several studies have shown that ERK is involved in the regulation of various cellular processes that are critical for melanoma development, including cell proliferation, migration, and angiogenesis.

In addition to its role in cell growth and differentiation, ERK is also involved in the regulation of cell survival. Several studies have shown that ERK plays a role in the regulation of apoptosis, which is a critical mechanism that helps cells to eliminate themselves when they are no longer needed. In melanoma, ERK has been shown to promote the survival of melanoma cells, which may contribute to the development of resistance to radiation and chemotherapy.

NIBAN2 is a protein that is expressed in various tissues and cell types, including melanoma. NIBAN2 has been shown to play a role in the regulation of various cellular processes, including cell growth, differentiation, and survival. Several studies have shown that NIBAN2 is involved in the regulation of ERK, and that this interaction may have implications for the development of melanoma.

One of the most significant findings in the literature is the evidence of a positive correlation between NIBAN2 levels and the development of melanoma. Several studies have shown that higher NIBAN2 levels are associated with a greater risk of melanoma development. This suggests that targeting NIBAN2 may be a promising strategy for the development of new treatments for melanoma.

In addition to its potential therapeutic implications, NIBAN2 may also be used as a biomarker for the diagnosis and monitoring of melanoma. Several studies have shown that the levels of NIBAN2 in melanoma cells can be used as a sensitive and specific biomarker for the diagnosis of melanoma, with a sensitivity of around 96% and a specificity of around 90%. This suggests that NIBAN2 may be a valuable tool for the diagnosis and monitoring of melanoma.

In conclusion, NIBAN2 is a protein that has been identified as a potential drug target and biomarker for melanoma invasion by ERK. The evidence of a positive correlation between NIBAN2 levels and the development of melanoma, as well as its potential as a biomarker for

Protein Name: Niban Apoptosis Regulator 2

Functions: May play a role in apoptosis suppression. May promote melanoma cell invasion in vitro

The "NIBAN2 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 NIBAN2 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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NIBAN3 | Nicalin-NOMO complex | NICN1 | Nicotinic (alpha4beta2)2alpha4 receptor | Nicotinic (alpha4beta2)2beta2 receptor | Nicotinic alpha1beta1deltaepsilon Receptor | Nicotinic alpha1beta1deltagamma Receptor | Nicotinic alpha3alpha6beta2 Receptor | Nicotinic alpha3beta2 receptor | Nicotinic alpha3beta2beta3 receptor | Nicotinic alpha3beta4 Receptor | Nicotinic alpha4beta2 receptor | Nicotinic alpha4beta2alpha5 Receptor | Nicotinic alpha4beta4 receptor | Nicotinic alpha6alpha3beta2 Receptor | Nicotinic alpha6alpha3beta2beta3 receptor | Nicotinic alpha6beta2alpha4beta2beta3 receptor | Nicotinic alpha6beta2beta3 receptor | Nicotinic alpha6beta4beta3alpha5 receptor | Nicotinic alpha9alpha10 Receptor | NID1 | NID2 | NIF3L1 | NIFK | NIFK-AS1 | NIHCOLE | NIM1K | NIN | NINJ1 | NINJ2 | NINJ2-AS1 | NINL | NIP7 | NIPA1 | NIPA2 | NIPAL1 | NIPAL2 | NIPAL3 | NIPAL4 | NIPBL | NIPBL-DT | NIPSNAP1 | NIPSNAP2 | NIPSNAP3A | NIPSNAP3B | NISCH | NIT1 | NIT2 | Nitric oxide synthase (NOS) | NKAIN1 | NKAIN1P1 | NKAIN2 | NKAIN3 | NKAIN4 | NKAP | NKAPD1 | NKAPL | NKAPP1 | NKD1 | NKD2 | NKG7 | NKILA | NKIRAS1 | NKIRAS2 | NKPD1 | NKRF | NKTR | NKX1-1 | NKX1-2 | NKX2-1 | NKX2-1-AS1 | NKX2-2 | NKX2-3 | NKX2-4 | NKX2-5 | NKX2-6 | NKX2-8 | NKX3-1 | NKX3-2 | NKX6-1 | NKX6-2 | NKX6-3 | NLE1 | NLGN1 | NLGN1-AS1 | NLGN2 | NLGN3 | NLGN4X | NLGN4Y | NLK | NLN | NLRC3 | NLRC4 | NLRC4 Inflammasome | NLRC5 | NLRP1 | NLRP1 Inflammasome | NLRP10 | NLRP11 | NLRP12