US2011183416A1PendingUtilityA1

Method of modulating the proliferation of medullary thyroid carcinoma cells

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Assignee: UBERTI ETTORE CIRO DEGLIPriority: Mar 6, 2001Filed: Jun 5, 2007Published: Jul 28, 2011
Est. expiryMar 6, 2021(expired)· nominal 20-yr term from priority
A61P 35/04A61K 38/31A61P 43/00A61P 35/00A61P 5/02A61K 38/08
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Claims

Abstract

The present invention is directed to a method of decreasing the rate of proliferation of medullary thyroid carcinoma cells which comprises contacting medullary thyroid carcinoma cells with one or more SSTR2 agonist. A preferred selective somatostatin receptor type-2 (SSTR-2) agonist cyclo[Tic-Tyr-D-Trp-Lys-Abu-Phe] is also disclosed.

Claims

exact text as granted — not AI-modified
1 . A method of modulating the rate of proliferation of medullary thyroid carcinoma cells (MTC) which comprises contacting MTC cells with one or more SSTR2 agonist and one or more somatostatin receptor subtype 5 (SSTR5) agonist, wherein said somatostatin receptor subtype 2 (SSTR2) agonist reduces the rate of proliferation of the MTC cells and said SSTR5 agonist attenuates the SSTR-2 agonist-induced reduction in cellular proliferation rate. 
     
     
         2 . A method according to  claim 1 , wherein said SSTR-5 agonist is D-Phe-Phe-Trp-D-Trp-Lys-Thr-Phe-Thr-NH 2  (SEQ ID NO: 1) or a pharmaceutically acceptable salt thereof. 
     
     
         3 . A compound of the formula cyclo[Tic-Tyr-D-Trp-Lys-Abu-Phe] (SEQ ID NO: 3). 
     
     
         4 . A selective somatostatin receptor type-2 (SSTR-2) agonist comprising the formula cyclo[Tic-Tyr-D-Trp-Lys-Abu-Phe] (SEQ ID NO: 3) or a pharmaceutically acceptable salt thereof.

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