Target Name: DPM3
NCBI ID: G54344
Other Name(s): MGC125904 | Testicular tissue protein Li 58 | Dolichyl-phosphate mannosyltransferase polypeptide 3 | dolichol-phosphate mannose synthase subunit 3 | MGC34275 | dolichyl-phosphate beta-D-mannosyltransferase subunit 3 | Mannose-P-dolichol synthase subunit 3 | dolichyl-phosphate mannosyltransferase subunit 3, regulatory | DPM3_HUMAN | Dolichol-phosphate mannose synthase subunit 3 | Dolichol-phosphate mannosyltransferase subunit 3 | mannose-P-dolichol synthase subunit 3 | DPM3 variant 1 | prostin 1 | Dolichyl-phosphate mannosyltransferase subunit 3, regulatory, transcript variant 2 | Dolichyl-phosphate mannosyltransferase subunit 3, regulatory, transcript variant 1 | Prostin 1 | Dolichol-phosphate mannosyltransferase subunit 3 (isoform 2) | MDDGB15 | DPM synthase complex subunit 3 | DPM3 variant 2 | MGC125905 | MPD synthase subunit 3 | CDG1O | DPM synthase subunit 3 | MDDGC15 | Prostin-1 | testicular tissue protein Li 58 | Dolichyl-phosphate beta-D-mannosyltransferase subunit 3 | Dolichol-phosphate mannosyltransferase subunit 3 (isoform 1) | dolichyl-phosphate mannosyltransferase polypeptide 3

DPM3: A Potential Drug Target and Biomarker

Drug resistance is a major problem in modern medicine, and new treatments are constantly being developed to overcome this issue. One potential solution to this problem is the development of drug targets, which are specific molecules within a cell that can be targeted with drugs to inhibit their function. One promising area of research is the identification of potential drug targets and biomarkers for various diseases, including cancer. In this article, we will focus on the potential drug target and biomarker DPM3, which has been identified as a potential drug target in the context of pancreatic ductal melanoma.

The Importance of DPM3 as a Drug Target

DPM3 is a protein that is expressed in the ducts of the pancreas, which are responsible for carrying insulin to the body's cells. In pancreatic ductal melanoma, the most common type of pancreatic cancer, the cells in the ducts of the pancreas grow out of control and can eventually form a tumor. This can lead to significant health complications, including the loss of vision and the need for pancreatic surgery.

DPM3 has been identified as a potential drug target because its expression is often increased in pancreatic ductal melanoma cells. Additionally, studies have shown that inhibiting the function of DPM3 has the potential to significantly reduce the growth of these cancer cells. This is exciting because it suggests that DPM3 could be a promising new treatment option for pancreatic ductal melanoma.

The Potential Benefits of Treating DPM3

If DPM3 is indeed a valid drug target, then treating pancreatic ductal melanoma cells with drugs that inhibit its function could lead to a significant improvement in patient outcomes. This is because pancreatic ductal melanoma is often treated with a combination of chemotherapy, radiation, and surgery. However, these treatments can often have significant side effects, and may not provide long-term remission for many patients.

By targeting DPM3 directly, a potential treatment could not only reduce the side effects associated with current treatments, but also potentially lead to a more effective response from the cancer cells. This could result in a more durable remission and improved quality of life for patients.

The Potential Risks of Treating DPM3

While the potential benefits of targeting DPM3 in pancreatic ductal melanoma are significant, there are also potential risks associated with this approach. One of the primary concerns is the potential for DPM3 to become a drug resistance gene, which could make the cancer more difficult to treat in the future.

Another potential risk is the potential for DPM3 to cause unintended consequences in other tissues. For example, if DPM3 is expressed in other organs or tissues, targeting it could have unintended effects on those cells as well.

Conclusion

In conclusion, DPM3 is a promising potential drug target and biomarker for pancreatic ductal melanoma. Its expression is often increased in pancreatic ductal melanoma cells, and inhibiting its function has the potential to significantly reduce the growth of these cancer cells. While there are potential risks associated with targeting DPM3, the potential benefits of this approach make it a promising area of research for the development of new treatments for pancreatic ductal melanoma.

Protein Name: Dolichyl-phosphate Mannosyltransferase Subunit 3, Regulatory

Functions: Stabilizer subunit of the dolichol-phosphate mannose (DPM) synthase complex; tethers catalytic subunit DPM1 to the endoplasmic reticulum

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