Target Name: GREM1
NCBI ID: G26585
Review Report on GREM1 Target / Biomarker Content of Review Report on GREM1 Target / Biomarker
GREM1
Other Name(s): cysteine knot superfamily 1, BMP antagonist 1 | Gremlin-1 | HMPS1 | DRM | GREMLIN | gremlin 1, cysteine knot superfamily, homolog | DUP15q | Gremlin 1, DAN family BMP antagonist, transcript variant 1 | Proliferation-inducing gene 2 protein | HMPS | gremlin 1, DAN family BMP antagonist | Gremlin 1-like protein | IHG-2 | down-regulated in Mos-transformed cells protein | Increased in high glucose protein 2 | colorectal adenoma and carcinoma 1 | CKTSF1B1 | MPSH | Gremlin 1, cysteine knot superfamily, homolog | PIG2 | gremlin 1-like protein | DAN domain family member 2 | Cysteine knot superfamily 1, BMP antagonist 1 | hereditary mixed polyposis syndrome | cell proliferation-inducing gene 2 protein | GREM1_HUMAN | GREM1 variant 1 | increased in high glucose-2 | Increased in high glucose-2 | Down-regulated in Mos-transformed cells protein | OTTHUMP00000159660 | Cell proliferation-inducing gene 2 protein | CRAC1 | Proliferation-inducing gene 2 | DAND2 | CRCS4 | C15DUPq

GREM1: A Potential Drug Target for Cancer and Neurodegenerative Diseases

GREM1 (cysteine knot superfamily 1, BMP antagonist 1) is a protein that has been identified as a potential drug target or biomarker for various diseases, including cancer, neurodegenerative diseases, and autoimmune disorders. Its unique structure and function have made it an attractive target for researchers to investigate, and its potential as a drug may have significant implications for the treatment of these diseases.

Structure and Function

GREM1 is a protein that is composed of 211 amino acid residues. It has a unique structure that is characterized by a cysteine knot, which is a type of protein structure that is composed of a series of interconnected amino acids that are held together by a disulfide bond. The cysteine knot is a structural feature that gives GREM1 its unique shape and stability.

In addition to its unique structure, GREM1 has several unique functions. It is a potent inhibitor of the bone-morphogenetic protein (BMP), which is a protein that plays a role in cell signaling and development. BMP is involved in many processes in the development and maintenance of tissues, including bone growth and wound healing. GREM1 has been shown to inhibit BMP activity, which may have potential implications for the treatment of conditions that are caused by over-active BMP signaling, such as cancer and neurodegenerative diseases.

Another function of GREM1 is its ability to block the activity of the protein called SMAD, which is a transcription factor that is involved in cell signaling. SMAD has been shown to play a role in the development and progression of many diseases, including cancer. GREM1 has been shown to inhibit the activity of SMAD, which may have implications for the treatment of these diseases.

GREM1 has also been shown to have anti-inflammatory effects, which may have implications for the treatment of autoimmune disorders. Inflammation is a natural response of the immune system, but in many cases, it can cause pain, swelling, and damage to tissues. GREM1 has been shown to inhibit the production of pro-inflammatory cytokines, which may have implications for the treatment of autoimmune disorders.

Potential Therapeutic Applications

GREM1's unique structure and functions make it an attractive target for the development of new drugs. Its ability to inhibit BMP and SMAD activity, as well as its anti-inflammatory effects, make it a potential drug target for a wide range of diseases.

One potential application for GREM1 is the treatment of cancer. Cancer is a disease that is characterized by the uncontrolled growth and spread of cells, and it is a leading cause of death in the world. Many cancers, including breast, lung, and ovarian cancers, are caused by the over-active activity of BMP and SMAD, and GREM1 has been shown to be a potent inhibitor of these proteins. By inhibiting the activity of BMP and SMAD, GREM1 may have implications for the treatment of these cancers.

Another potential application for GREM1 is the treatment of neurodegenerative diseases. Neurodegenerative diseases, such as Alzheimer's and Parkinson's diseases, are characterized by the progressive loss of brain cells and the development of neurofibrillary tangles. GREM1 has been shown to inhibit the production of pro-inflammatory cytokines, which may have implications for the treatment of these diseases.

GREM1 may also be a potential biomarker for some diseases. Its unique structure and functions make it an attractive target for the development of new diagnostic tools. For example, GREM1 may be used as a biomarker for the diagnosis of cancer, as its expression is often reduced in cancer cells compared to healthy cells.

Conclusion

GREM1 is a protein that has unique structure and functions that make it an attractive target for the development of new drugs. Its ability to inhibit the activity of BMP and SMAD, as well as its anti-inflammatory effects, make it a potential drug

Protein Name: Gremlin 1, DAN Family BMP Antagonist

Functions: Cytokine that may play an important role during carcinogenesis and metanephric kidney organogenesis, as a BMP antagonist required for early limb outgrowth and patterning in maintaining the FGF4-SHH feedback loop. Down-regulates the BMP4 signaling in a dose-dependent manner (By similarity). Antagonist of BMP2; inhibits BMP2-mediated differentiation of osteoblasts (in vitro) (PubMed:27036124). Acts as inhibitor of monocyte chemotaxis. Can inhibit the growth or viability of normal cells but not transformed cells when is overexpressed (By similarity)

The "GREM1 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 GREM1 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

More Common Targets

GREM1-AS1 | GREM2 | GREP1 | GRHL1 | GRHL2 | GRHL3 | GRHL3-AS1 | GRHPR | GRIA1 | GRIA2 | GRIA3 | GRIA4 | GRID1 | GRID2 | GRID2IP | GRIFIN | GRIK1 | GRIK1-AS1 | GRIK1-AS2 | GRIK2 | GRIK3 | GRIK4 | GRIK5 | GRIN1 | GRIN2A | GRIN2B | GRIN2C | GRIN2D | GRIN3A | GRIN3B | GRINA | GRIP1 | GRIP2 | GRIPAP1 | GRK1 | GRK2 | GRK3 | GRK4 | GRK5 | GRK6 | GRK7 | GRM1 | GRM2 | GRM3 | GRM4 | GRM5 | GRM5-AS1 | GRM5P1 | GRM6 | GRM7 | GRM7-AS3 | GRM8 | GRM8-AS1 | GRN | Growth Factor Receptor-Bound Protein | GRP | GRPEL1 | GRPEL2 | GRPEL2-AS1 | GRPR | GRSF1 | GRTP1 | GRTP1-AS1 | GRWD1 | GRXCR1 | GRXCR2 | GS1-24F4.2 | GS1-600G8.3 | GSAP | GSC | GSC2 | GSDMA | GSDMB | GSDMC | GSDMD | GSDME | GSE1 | GSEC | GSG1 | GSG1L | GSG1L2 | GSK3A | GSK3B | GSKIP | GSN | GSPT1 | GSPT2 | GSR | GSS | GSTA1 | GSTA12P | GSTA2 | GSTA3 | GSTA4 | GSTA5 | GSTA7P | GSTCD | GSTK1 | GSTM1 | GSTM2