Target Name: ST7L
NCBI ID: G54879
Other Name(s): Suppressor of tumorigenicity 7 protein-like | ST7L_HUMAN | OTTHUMP00000013496 | tumor suppressor ST7 like | ST7R | OTTHUMP00000013494 | Suppression of tumorigenicity 7 like, transcript variant 1 | FAM4B | OTTHUMP00000013495 | FLJ11657 | OTTHUMP00000013493 | Suppressor of tumorigenicity 7 protein-like (isoform 4) | ST7L variant 4 | OTTHUMP00000013490 | Suppressor of tumorigenicity 7 protein-like (isoform 1) | ST7-related protein | OTTHUMP00000013491 | ST7L variant 1 | OTTHUMP00000013492 | Tumor suppressor ST7 like | STLR | suppression of tumorigenicity 7 like | Suppression of tumorigenicity 7 like, transcript variant 4 | FLJ20284 | OTTHUMP00000013497

A Promising Drug Target: ST7L (Suppressor of tumorigenicity 7 Protein-Like)

ST7L (Suppressor of tumorigenicity 7 protein-like) is a protein that has been identified as a potential drug target or biomarker for various diseases, including cancer. TheSuppressor of tumorigenicity 7 protein is a non-coding RNA molecule that has been shown to regulate the activity of several oncogenic genes, thereby promoting the growth and proliferation of cancer cells. ST7L has also been shown to play a role in the development and progression of various diseases, including neurodegenerative disorders and autoimmune diseases.

The Identification of ST7L

ST7L was first identified as a novel gene that encodes a protein with significant homology to the tumor suppressor protein p53. Thep53 is a well-known gene that has been shown to play a critical role in the regulation of cell growth and the apoptosis process, which is a natural response to DNA damage. Thep53 gene has been implicated in the development of many diseases, including cancer.

Subsequent studies have shown that ST7L is highly expressed in various tissues and that it is involved in the regulation of cellular processes that are critical for the development and maintenance of cancer. ST7L has also been shown to interact with several other proteins, including T-cell factor, which is a well-known signaling molecule that plays a critical role in the regulation of immune responses and cancer development.

The Potential Druggability of ST7L

The potential druggability of ST7L makes it an attractive target for cancer therapy. One of the main reasons for its potential drugability is its ability to interact with multiple signaling pathways, including the T-cell factor signaling pathway. This allows for the development of small molecules or antibodies that can specifically target ST7L and inhibit its activity, thereby triggering cellular responses that are targeted to cancer cells.

Another reason for the potential druggability of ST7L is its well-established role in the regulation of cell growth and the apoptosis process. Many drugs that are currently in use for cancer treatment work by inhibiting the activity of signaling pathways that promote cell growth and survival. By targeting ST7L, these drugs can disrupt the signaling pathways that promote cancer cell growth and proliferation, leading to a reduction in the size and number of cancer cells.

The Potential Applications of ST7L as a Drug Target or Biomarker

The potential applications of ST7L as a drug target or biomarker are vast and varied. In cancer therapy, ST7L can be used to target cancer cells that have increased levels of ST7L. This can lead to the inhibition of signaling pathways that promote cancer cell growth and proliferation, leading to a reduction in the size and number of cancer cells.

In addition to its potential for cancer therapy, ST7L has also been identified as a potential biomarker for various diseases, including cancer. Its well-established role in the regulation of cell growth and the apoptosis process makes it an attractive target for diagnostic tests that are designed to measure the levels of ST7L in various tissues and fluids.

Conclusion

In conclusion, ST7L is a protein that has been identified as a potential drug target or biomarker for various diseases, including cancer. Its ability to interact with multiple signaling pathways and its well-established role in the regulation of cellular processes that are critical for the development and maintenance of cancer make it an attractive target for therapeutic intervention. Further research is needed to fully understand the potential applications of ST7L as a drug target or biomarker, and to develop safe and effective therapies that can be used to treat

Protein Name: Suppression Of Tumorigenicity 7 Like

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ST8SIA1 | ST8SIA2 | ST8SIA3 | ST8SIA4 | ST8SIA5 | ST8SIA6 | ST8SIA6-AS1 | STAB1 | STAB2 | STAC | STAC2 | STAC3 | STAG1 | STAG2 | STAG3 | STAG3L1 | STAG3L2 | STAG3L3 | STAG3L4 | STAG3L5P | STAG3L5P-PVRIG2P-PILRB | STAGA complex | Stage selector protein complex | STAM | STAM-DT | STAM2 | STAMBP | STAMBPL1 | STAP1 | STAP2 | STAR | STARD10 | STARD13 | STARD3 | STARD3NL | STARD4 | STARD4-AS1 | STARD5 | STARD6 | STARD7 | STARD7-AS1 | STARD8 | STARD9 | STARP1 | STAT1 | STAT2 | STAT3 | STAT4 | STAT4-AS1 | STAT5 | STAT5A | STAT5B | STAT6 | STATH | STAU1 | STAU2 | STAU2-AS1 | STBD1 | STC1 | STC2 | STEAP1 | STEAP1B | STEAP2 | STEAP2-AS1 | STEAP3 | STEAP3-AS1 | STEAP4 | STEEP1 | Steroid 5-alpha-Reductase | Sterol O-acyltransferase (ACAT) | Sterol Regulatory Element-Binding Protein | STH | STIL | STIM1 | STIM2 | STIMATE | STIN2-VNTR | STING1 | STIP1 | STK10 | STK11 | STK11IP | STK16 | STK17A | STK17B | STK19 | STK24 | STK25 | STK26 | STK3 | STK31 | STK32A | STK32A-AS1 | STK32B | STK32C | STK33 | STK35 | STK36 | STK38 | STK38L