Target Name: TARM1
NCBI ID: G441864
Other Name(s): T cell-interacting, activating receptor on myeloid cells 1 | OSCAR-like transcript-2 protein | T cell-interacting, activating receptor on myeloid cells 1, transcript variant 1 | T cell-interacting, activating receptor on myeloid cells 1, transcript variant 2 | T-cell-interacting, activating receptor on myeloid cells protein 1 (isoform 1) | TARM1 variant 1 | T-cell-interacting, activating receptor on myeloid cells protein 1 (isoform 2) | TARM1_HUMAN | T-cell-interacting, activating receptor on myeloid cells protein 1 | TARM1 variant 2 | OLT-2

TARM1: A Potential Drug Target for T Cells and Myeloid Cells

T cells and myeloid cells are key immune cells that play crucial roles in fighting against infections, cancer, and other diseases. They are part of the adaptive immune system, which is responsible for protecting the body against a wide range of threats. T cells, in particular, are involved in cell-mediated immunity, as they recognize and respond to foreign antigens in the body. Myeloid cells, on the other hand, are responsible for producing antibodies, which are proteins that help to neutralize pathogens and cancer cells.

T cell-interacting, activating receptor (TARM1) is a protein that is expressed in T cells and myeloid cells. It is a G protein-coupled receptor (GPCR), which means that it interacts with intracellular signaling molecules called G proteins. TARM1 is involved in cell signaling, particularly in the regulation of cell growth, differentiation, and survival.

Drugs that target TARM1 have the potential to be effective in treating a wide range of diseases, including cancer, autoimmune disorders, and infections. In this article, we will explore the potential of TARM1 as a drug target and discuss the implications of targeting this protein in medical research and clinical practice.

Targeting TARM1: A novel therapeutic approach

TARM1 is a protein that is expressed in both T cells and myeloid cells. It is involved in cell signaling and has been implicated in the regulation of both T cell and myeloid cell function. This makes it an attractive target for drug development, particularly for diseases that involve T cells or myeloid cells.

One of the challenges in targeting TARM1 is its widespread expression across different cell types. Unlike many other GPCRs, TARM1 is not highly expressed in a specific cell type, and it is not well-studied in cell-cell interactions. This makes it difficult to identify potential drug targets and determine the efficacy of potential therapies.

However, recent studies have identified potential targets for TARM1. One of these studies identified a potential drug target for TARM1, which is located on the protein kinase CKL2 (CKL2 kinase). CKL2 is a protein that is involved in the regulation of cell growth and has been implicated in the development of cancer.

Another study identified a potential drug target for TARM1, which is located on the transcription factor NF-E2F3. NF-E2F3 is a protein that is involved in the regulation of gene expression and has been implicated in the development of cancer.

Targeting TARM1: Potential clinical applications

The identification of potential drug targets for TARM1 has significant implications for the development of new therapies. If TARM1 is successfully targeted, it could lead to the development of new treatments for a wide range of diseases, including cancer, autoimmune disorders, and infections.

For example, targeting TARM1 with small molecules or antibodies could be effective in treating a variety of cancers, including breast, lung, and ovarian cancers. This could be achieved by inhibiting the activity of TARM1, which would reduce the signaling of T cells and myeloid cells.

Targeting TARM1 could also be effective in treating autoimmune disorders, such as rheumatoid arthritis and lupus. In these disorders, T cells become activated and produce antibodies that target the body's own tissues. Targeting TARM1 could be achieved by inhibiting the activity of T cells, which would reduce their production of antibodies.

In addition, targeting TARM1 could be

Protein Name: T Cell-interacting, Activating Receptor On Myeloid Cells 1

Functions: May act as receptor (By similarity). Negatively regulates TCR-mediated CD4(+) T cell proliferation and activation, possibly by binding an unknown ligand on the T cell surface (PubMed:26311901). Enhances Toll-like receptor-mediated production of pro-inflammatory cytokines by macrophages and neutrophils (By similarity)

More Common Targets

TARP | TARS1 | TARS2 | TARS3 | TAS1R1 | TAS1R2 | TAS1R3 | TAS2R1 | TAS2R10 | TAS2R13 | TAS2R14 | TAS2R16 | TAS2R19 | TAS2R20 | TAS2R3 | TAS2R30 | TAS2R31 | TAS2R38 | TAS2R39 | TAS2R4 | TAS2R40 | TAS2R41 | TAS2R42 | TAS2R43 | TAS2R45 | TAS2R46 | TAS2R5 | TAS2R50 | TAS2R60 | TAS2R63P | TAS2R64P | TAS2R7 | TAS2R8 | TAS2R9 | TASL | TASOR | TASOR2 | TASP1 | Taste receptor type 2 | Taste Receptors Type 1 | TAT | TAT-AS1 | TATDN1 | TATDN2 | TATDN2P3 | TATDN3 | TAX1BP1 | TAX1BP3 | TBATA | TBC1D1 | TBC1D10A | TBC1D10B | TBC1D10C | TBC1D12 | TBC1D13 | TBC1D14 | TBC1D15 | TBC1D16 | TBC1D17 | TBC1D19 | TBC1D2 | TBC1D20 | TBC1D21 | TBC1D22A | TBC1D22A-AS1 | TBC1D22B | TBC1D23 | TBC1D24 | TBC1D25 | TBC1D26 | TBC1D27P | TBC1D28 | TBC1D29P | TBC1D2B | TBC1D3 | TBC1D30 | TBC1D31 | TBC1D32 | TBC1D3B | TBC1D3C | TBC1D3F | TBC1D3G | TBC1D3H | TBC1D3L | TBC1D3P1 | TBC1D3P2 | TBC1D4 | TBC1D5 | TBC1D7 | TBC1D8 | TBC1D8-AS1 | TBC1D8B | TBC1D9 | TBC1D9B | TBCA | TBCB | TBCC | TBCCD1 | TBCD | TBCE