Cancer is a major global burden of disease and public health concern. Nearly 1.7 million people in the US are diagnosed with cancer every year, while in China, as many as 3.5 million new cancer patients are diagnosed every year. ScinnoHub strives to develop innovative small-molecule drugs, including protein kinase inhibitors (e.g. cyclin-dependent kinase inhibitors and tyrosine kinase inhibitors) and MAT2A inhibitors as well as radionuclide-drug conjugates to treat various types of cancers.
Lymphoma is a group of over 90 malignant neoplasms of lymphocytes, which is typically classified as non-Hodgkin or Hodgkin lymphomas. Hodgkin lymphoma tends to have favorable prognosis. Non-Hodgkin lymphoma, in contrast, is the most common hematological malignancy worldwide, affecting approximately 1.5 million people and accounting for nearly 3% of cancer diagnoses and deaths. Bruton's tyrosine kinase (BTK) is a key component of the B-cell receptor (BCR) signaling pathway and plays an essential role in B-cell maturation and lymphomagenesis. To date, five irreversible BTK inhibitors have been approved to treat different types of lymphomas.
Prostate cancer is the third most common diagnosed malignancy. Although clinically localized prostate cancer can be treated with radical prostatectomy or radiotherapy, the prognosis for metastatic castration-resistant prostate cancer (mCRPC) remains poor. Radioligand therapy, which targets and delivers tumor-killing radiation to cancer cells, is a promising treatment for mCRPC.
Prostate-specific membrane antigen (PSMA) is significantly overexpressed (up to 1000-fold) by prostate cancer cells and its expression level correlates with the stage of cancer and grade of tumor, which enables it to sever as a potential biomarker for targeted radioligand therapy. So far, various PSMA-targeted radioligands have been developed to treat prostate cancer, including 177Lu-PSMA-617 (approved), 177Lu- PSMA I&T (Phase 2) and 177Lu-CTT-1403 (Phase 1).
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