In addition to the classical neurotransmitters, acetylcholine and noradrenaline, a wide number of peptides with neurotransmitter activity have been identified in the past few years. Among them, the tachykinins substance P (SP), neurokinin A (NKA) and neurokinin B (NKB) appear to act as mediators of nonadrenergic, noncholinergic (NANC) excitatory neurotransmission. Tachykinins interact with specific membrane proteins, belonging to the family of G protein-coupling cell membrane receptors. Until now, three tachykinin receptors termed NK1 (NK1R), NK2 (NK2R) and NK3 (NK3R) have been cloned in different species. A large amount of reports suggests that these peptides are involved in nociception and neuroimmunomodulation, and in the development of different diseases such as bronchial asthma, inflammatory bowel syndrome and psychiatric disorders. Tachykinin receptor antagonists are therefore promising, therapeutically relevant agents. However, and in spite of extensive research, the obtention of selective antagonists of tachykinin receptors have revealed very difficult. An understanding of how ligands interact with their receptors is essential to permit a rational design of compounds acting selectively at the tachykinin receptor level. The major aim of the present article is to review the structure-activity data that exist for tachykinins and their receptors, with the purpose of getting insight into basic structural requirements that determine ligand/receptor interaction.

Genetic alterations serve as beacons for the involvement of specific pathways in tumorigenesis. It was previously shown that 5% of prostate tumors harbor CTNNB1 mutations, suggesting that this tumor type may involve a deregulated APC/CTNNB1 pathway. To explore this possibility further, we searched for mutations in genes implicated in this pathway in 22 samples that included cell lines, xenografts, and primary tumors. We identified seven alterations: two in CTNNB1, three in APC, and two in hTRCP1 (also known as BTRC) which controls the degradation of CTNNB1. Alterations in the CTNNB1 regulatory domain, APC, and hTRCP1 were mutually exclusive, consistent with their equivalent effects on CTNNB1 stability. These results suggest that CTNNB1 signaling plays a critical role in the development of a significant fraction of prostate cancers. Moreover, they provide the first evidence that hTRCP1 plays a role in human neoplasia.

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This work was supported by grants from Ministerio de Economía y Competitividad (CTQ2011-25564 and BFI2011-25021) and Junta de Andalucía (P08-CVI-04185), Spain. J.G.-O., F.M.P., M.F.-S., N.P., A.C.-R., T.A.A., M.H., M.R., M.T.-S. and L.C. have nothing to declare.

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Laparocerus are plant‐chewing flightless weevils distributed on oceanic islands in Macaronesia, with a single species in Morocco. The genus has a complicated taxonomic history with several subgenera described. To assist in a taxonomical revision of the group, a molecular study was undertaken. In this first contribution, the species from the Azores and Madeira archipelagos are studied together with representatives of subgenera from the Canary Islands and the single known continental species (46 OTUs). Phylogenetic analyses are based on sequence data from mitochondrial cytochrome oxidase II (COII) and the ribosomal 16S ribosomal RNA (16S rRNA) genes (combined data set 1023 bp), with additional data from the nuclear elongation factor 1α (EF‐1α) for some selected species. Maximum likelihood (ML) and Bayesian analyses show that all Madeiran species are monophyletic and form a monophyletic group with the Afro‐Canarian samples. Species of the genus Lichenophagus appear within the Madeiran and Canarian Laparocerus clades, but separated in accordance with their respective island origin. Thus, Lichenophagus is here restricted to Madeiran species and proposed as subgenus (status novo) of Laparocerus. Conversely, the Laparocerus subgenus Drouetius from the Azores is revealed to be a separate and distant outgroup, in agreement with its morphological distinctiveness, deserving an independent genus status. Internal relationships within the Madeiran clade are discussed and compared with morphologically defined species groups. The Madeiran monotypic subgenus Cyphoscelis is not supported by the genetic data and synonymized (nov. syn.) with Laparocerus. Subgenera Laparocerus and Atlantis prove to be polyphyletic. Consequently a restriction to monophyletic and morphologically congruent clades is proposed. A cryptic species vicariant of Laparocerus morio was detected and recognized as L. chaoensis, status novo. Other cases of discrepancy between the genetic results and the traditional taxonomy are discussed in detail in the light of mitochondrial introgression, incomplete lineage sorting or poor taxonomy hypotheses.

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