Cell expansion and
metastasis are considered hallmarks of tumour progression. Therefore, efforts have been made to develop novel anti-
cancer drugs that inhibit both the proliferation and the motility of tumour cells. Synthetic alkylphospholipids, compounds with aliphatic side chains that are
ether linked to a
glycerol backbone, are structurally derived from
platelet-activating factor and represent a new class of drugs with anti-proliferative properties in tumour cells. These compounds do not interfere with the
DNA or mitotic spindle apparatus of the cell. Instead, they are incorporated into cell membranes, where they accumulate and interfere with lipid metabolism and
lipid-dependent signalling pathways. Recently, it has been shown that the most commonly studied alkylphospholipids inhibit proliferation by inducing apoptosis in malignant cells while leaving normal cells unaffected. This review focuses on a novel group of synthetic alkylphospholipids, the glycosidated
phospholipids, which contain
carbohydrates or
carbohydrate-related molecules at the sn-2 position of the
glycerol backbone. Members of this subfamily also exhibit anti-proliferative capacity and modulate the cell adhesion, differentiation, and migration of tumour cells. Among this group,
Ino-C2-PAF shows the highest efficacy and low cytotoxicity. Apart from its anti-proliferative effect,
Ino-C2-PAF strongly reduces cell motility via its inhibitory effect on the phosphorylation of the cytosolic
tyrosine kinases FAK and Src. Signalling pathways under the control of the FAK/Src complex are normally required for both migration and proliferation and play a prominent role in tumour progression. We intend to highlight the potential of glycosidated
phospholipids, especially
Ino-C2-PAF, as a promising new group of drugs for the treatment of hyperproliferative and migration-based
skin diseases.