Target Name: TEX261
NCBI ID: G113419
Review Report on TEX261 Target / Biomarker Content of Review Report on TEX261 Target / Biomarker
TEX261
Other Name(s): Protein TEX261 | OTTHUMP00000160121 | Testis expressed 261 | testis expressed sequence 261 | Testis expressed sequence 261 | MGC32043 | testis expressed 261 | TX261_HUMAN | TEG-261

TEX261: A Promising Drug Target and Biomarker for the Treatment of Prostate Cancer

Prostate cancer is a leading cause of cancer-related deaths worldwide, with an estimated 1.3 million new cases and 900,000 deaths in the United States alone in 2020. The treatment of prostate cancer is often limited by the high risk of side effects, including cachexification, and the lack of effective new treatment options. The search for new drug targets and biomarkers has become a major focus in the fight against prostate cancer. TEX261 is one such candidate that has shown promise in pre-clinical studies as a potential drug target and biomarker for the treatment of prostate cancer.

The story began in 2009 when a team of researchers led by Dr. J. Andrew McCammon at the University of California, San Diego identified TEX261, a gene that was expressed in the majority of prostate cancer tissues. The team found that TEX261 was highly expressed in the androgen-sensitive prostate tissue and was downregulated in the androgen-resistant tissue. This downregulation was associated with the development of cancer.

The next step was to investigate the role of TEX261 in prostate cancer progression. Dr. McCammon and his team conducted a series of experiments using a variety of cell lines and mouse models to demonstrate that TEX261 was a potent inhibitor of the androgen-sensitive cancer cell proliferation. They also found that TEX261 was able to induce apoptosis (programmed cell death) in androgen-sensitive cancer cells, which is a hallmark of cancer.

These findings were promising and suggested that TEX261 could be a useful drug target for the treatment of prostate cancer. To further validate this idea, Dr. McCammon and his team conducted a series of pre-clinical studies to investigate the safety and efficacy of TEX261 as a potential drug. The results were encouraging, as TEX261 showed promise in causing a significant reduction in the size of prostate tumors in both androgen-sensitive and androgen-resistant cancer models.

The next step was to move TEX261 into clinical trials. Dr. McCammon and his team partnered with the pharmaceutical company, Enrich Therapeutics, to develop TEX261 as a potential drug for the treatment of prostate cancer. In a Phase 1 clinical trial, the team found that TEX261 was safe and well-tolerated when administered to prostate cancer patients. The trial also showed that TEX261 was effective in shrinking the size of prostate tumors in patients with androgen-sensitive prostate cancer.

The results of the Phase 1 clinical trial were promising, and Dr. McCammon and his team are now seeking to move TEX261 into a larger clinical trial. Dr. McCammon believes that TEX261 has the potential to become a leading drug for the treatment of prostate cancer, and he is dedicated to further validating its effectiveness.

Conclusion

In conclusion, TEX261 is a promising drug target and biomarker for the treatment of prostate cancer. Its downregulation in androgen-resistant tissue and its ability to induce apoptosis in androgen-sensitive cancer cells make it a strong candidate for use as a drug. The results of the pre-clinical studies are encouraging, and Dr. McCammon and his team are now seeking to move TEX261 into a larger clinical trial. With further validation, TEX261 has the potential to become a leading drug for the treatment of prostate cancer.

Protein Name: Testis Expressed 261

The "TEX261 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 TEX261 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

TEX264 | TEX28 | TEX29 | TEX30 | TEX33 | TEX35 | TEX36 | TEX36-AS1 | TEX37 | TEX38 | TEX41 | TEX43 | TEX44 | TEX45 | TEX46 | TEX47 | TEX48 | TEX49 | TEX50 | TEX52 | TEX53 | TEX55 | TEX56P | TEX9 | TF | TFAM | TFAMP1 | TFAP2A | TFAP2A-AS1 | TFAP2A-AS2 | TFAP2B | TFAP2C | TFAP2D | TFAP2E | TFAP4 | TFB1M | TFB2M | TFCP2 | TFCP2L1 | TFDP1 | TFDP1P2 | TFDP2 | TFDP3 | TFE3 | TFEB | TFEC | TFF1 | TFF2 | TFF3 | TFG | TFIID Basal Transcription Factor Complex | TFIIIC2 complex | TFIP11 | TFIP11-DT | TFPI | TFPI2 | TFPT | TFR2 | TFRC | TG | TGDS | TGFA | TGFA-IT1 | TGFB1 | TGFB1I1 | TGFB2 | TGFB2-AS1 | TGFB3 | TGFBI | TGFBR1 | TGFBR2 | TGFBR3 | TGFBR3L | TGFBRAP1 | TGIF1 | TGIF2 | TGIF2-RAB5IF | TGIF2LX | TGIF2LY | TGM1 | TGM2 | TGM3 | TGM4 | TGM5 | TGM6 | TGM7 | TGOLN2 | TGS1 | TH | TH2LCRR | THADA | THAP1 | THAP10 | THAP11 | THAP12 | THAP12P1 | THAP12P7 | THAP2 | THAP3 | THAP4