For many frog species that aggregate around ponds or streams, chorus attendance, the percentage of time or nights a given male is present and actively calling at an aggregation, is the strongest documented predictor of inter‐male variation in reproductive success in the wild. Males are, thus, thought to compete via endurance rivalry, where available energetic reserves and individual physiology interact to determine chorus tenure. Frogs often exhibit territorial behavior within these aggregations, and territorial status is likely to influence a male's rate of energy expenditure. While males of several anuran species have been shown to hold territories across nights, it is not well understood whether such calling site fidelity is correlated with chorus attendance or mating success. Using subdermal RFID (PIT) tags to minimize disturbance to chorus structure, we quantified site fidelity, chorus attendance, and mating success for all male red‐eyed treefrogs (Agalychnis callidryas) within a breeding aggregation in Panama across 50 consecutive nights. We found that nearly half of these males held territories across nights, that this cross‐night territorial behavior was highly correlated with chorus attendance, and that chorus attendance was, in turn, the strongest predictor of male mating success. Males were most faithful to calling sites containing vegetation contiguous with adjacent sites and were more likely to remain at a site if they were successful in acquiring a mate there on the previous night. To our knowledge, this is the first study linking male site fidelity to chorus attendance and mating success in anurans. While female mate choice is an established driver of lineage diversification and the evolution of sexual signals, agonistic interactions between males at breeding aggregations are well‐documented from a wide range of anuran taxa. The relationship between male–male interactions and mating success deserves broader research attention among anuran species.
RUNX2, a transcription factor, initially known for its indispensable role in skeletal development. RUNX2 is essential for osteoblast differentiation and the maintain of the osteocyte balance. RUNX2 acts directly on osteoblasts via Fgf pathway or on mesenchymal progenitors through Hedgehog, Wnt, Pthlh and DLX5. Currently, many reports point its critical role in the progression and metastasis of several cancer types. RUNX2 is involved in EMT process, invasion and metastasis through the modulation of important oncogenic pathways, including Wnt, FAK/PTK and AKT. In melanoma, RUNX2 is a key player in mediating intrinsic RTK-associated pro-oncogenic properties. We have showed a dramatic up regulation of RUNX2 expression with concomitant up-regulation of EGFR, IGF-1R and AXL, in melanoma cells rendered resistant to BRAF mutant inhibitors. Approximately half of melanomas carry BRAF mutations which enhance tumor invasion and metastasis. In this chapter, we describe the potential mechanisms, leading to the upregulation of RUNX2 in melanoma with BRAF mutations. We also highlight the critical role of PI3K/AKT in the expression and activation of RUNX2, and its consequences on the regulation of many critical factors, controlling cancer invasion and metastasis.
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