Recent research revealed that mutations in ras genes contribute to tumorigenesis in a number of tissues. In order to achieve a biologically active state during mitosis, Ras proteins need to undergo a number of post-translational modifications of which farnesylation is the most important one. Mutation of ras genes blocks the physiological dephosphorylating process of Ras proteins. This can result in tumour development and growth. Inhibition of farnesylation by farnesyltransferase inhibitors may prevent these processes. Several types of farnesyltransferase inhibitors have been developed, each with its own unique mechanism of interference. Pre-clinical studies revealed promising tumour regression in several models as well as limited side-effec...
Farnesyl transferase inhibitors (FTIs) have emerged as promising leads in the search for rationally ...
Mutations of RAS oncogenes are responsible for about 30% of all human cancer types, including pancre...
Farnesyl transferase inhibitors (FTIs) have emerged as promising leads in the search for rationally ...
Over the last decades, knowledge on the genetic defects involved in tumor formation and growth has i...
The targeting of molecular abnormalities in neoplasms may provide an opportunity to improve the sele...
Oncogenic Ras proteins have been seen as an important target for novel anticancer drugs. Due to the ...
Local recurrence after a definitive course of radiation therapy remains a significant clinical probl...
Activating RAS mutations are found in a subset of fusion-negative rhabdomyosarcoma (FN-RMS), and the...
Recently developed CAAX peptidomimetic compounds have been shown to be potent and specific inhibitor...
Recently developed CAAX peptidomimetic compounds have been shown to be potent and specific inhibitor...
AbstractProteins that transmit abnormal growth signals offer enticing points of intervention for the...
The Ras family of small GTPases (N-, H-, and K-Ras) is a group of important signaling mediators. Ras...
Inhibitors of the enzyme farnesyl protein transferase prevent a key step in the post-translational p...
The ras family of proto-oncogenes are upstream mediators of several essential cellular signal transd...
Ras proteins are small GTPases that regulate key pathways involved in cell growth, proliferation and...
Farnesyl transferase inhibitors (FTIs) have emerged as promising leads in the search for rationally ...
Mutations of RAS oncogenes are responsible for about 30% of all human cancer types, including pancre...
Farnesyl transferase inhibitors (FTIs) have emerged as promising leads in the search for rationally ...
Over the last decades, knowledge on the genetic defects involved in tumor formation and growth has i...
The targeting of molecular abnormalities in neoplasms may provide an opportunity to improve the sele...
Oncogenic Ras proteins have been seen as an important target for novel anticancer drugs. Due to the ...
Local recurrence after a definitive course of radiation therapy remains a significant clinical probl...
Activating RAS mutations are found in a subset of fusion-negative rhabdomyosarcoma (FN-RMS), and the...
Recently developed CAAX peptidomimetic compounds have been shown to be potent and specific inhibitor...
Recently developed CAAX peptidomimetic compounds have been shown to be potent and specific inhibitor...
AbstractProteins that transmit abnormal growth signals offer enticing points of intervention for the...
The Ras family of small GTPases (N-, H-, and K-Ras) is a group of important signaling mediators. Ras...
Inhibitors of the enzyme farnesyl protein transferase prevent a key step in the post-translational p...
The ras family of proto-oncogenes are upstream mediators of several essential cellular signal transd...
Ras proteins are small GTPases that regulate key pathways involved in cell growth, proliferation and...
Farnesyl transferase inhibitors (FTIs) have emerged as promising leads in the search for rationally ...
Mutations of RAS oncogenes are responsible for about 30% of all human cancer types, including pancre...
Farnesyl transferase inhibitors (FTIs) have emerged as promising leads in the search for rationally ...