New drug to treat deadly skin cancer in the offing

SBI-756 shows promise for treating serious forms of carcinoma, such as melanoma.

November 26, 2015 01:42 pm | Updated August 10, 2016 03:09 pm IST - WASHINGTON:

SBI-756 shows promise for treating deadly forms of skin cancer, such as melanoma (in the picture), which are resistant to existing therapies.

SBI-756 shows promise for treating deadly forms of skin cancer, such as melanoma (in the picture), which are resistant to existing therapies.

Scientists have discovered a new drug that shows promise for treating deadly forms of skin cancer, such as melanoma, which are resistant to existing therapies.

The new compound, named SBI-756, targets a specific molecular machine known as the translation initiation complex. These structures are in every cell and play the critical role of translating messenger RNA (mRNA) into proteins. In cancer cells the complex is impaired, producing extra protein and providing a growth advantage to tumours.

Inhibiting tumour growth

SBI-756 causes the translation complex to dissociate, and inhibit melanoma cell growth.

“A major issue limiting the effectiveness of current melanoma therapies is that tumours become resistant to treatment,” said Ze’ev Ronai from Sanford Burnham Prebys Medical Discovery Institute (SBP) in US.

“Combining drugs that come at a melanoma from different angles may help overcome the problem of drug resistance,” said Ronai.

Caused by mutations in specific gene

About 50 per cent of melanomas are caused by mutations in a specific gene called BRAF. Patients with these tumours are commonly prescribed vemurafenib, a BRAF inhibitor that shrinks tumours.

However, many patients experience a relapse within weeks, months, or even years because tumours evolve and become resistant to the drug.

A similar phenomenon is seen in mice, where treatment of BRAF melanomas results in an initial response, but 3 to 4 weeks later the tumours return.

Combination does the trick

The team found that if SBI-756 is co-administered with vemurafenib, the tumours disappeared and did not reoccur.

Even in mice with advanced or late stage BRAF-driven cancer, the reappearance of resistant tumours was slowed by including SBI-756.

Significant advantage

These data suggests that SBI-756 provides a significant advantage in overcoming tumour resistance.

In other forms of melanoma, caused by mutations in the genes NRAS and NF1 — which are known as unresponsive to BRAF drugs — administering SBI-756 alone significantly lessened the tumour load, the scientists found.

The team is now testing whether combining SBI-756 with existing drugs used for treating these types of melanomas can make the tumours disappear.

Possibly for neurodegenerative diseases

“The finding of SBI-756 is also exciting for the possible treatment of diseases other than cancer, such as neurodegenerative diseases, where the activity of the translation initiation complex is reported to be higher,” said Professor Nahum Sonenberg of McGill University.

The study was published in the journal Cancer Research .

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