RESUMEN
Castration-resistant prostate cancer (CRPC) development is the foremost concern after treatment of patients with high risk with locally advanced or metastatic prostate cancer. Androgen receptor (AR) is the main driver of CRPC development, through its interaction with epigenetic modifier genes, placing epigenetics modifications in the forefront of CRPC development. Comparing the DNA methylation and expression profile of androgen-sensitive and -refractory prostate cancer cells, we describe the epigenetic silencing of claudin-3 (CLDN3) in AR positive cells resistant to androgen deprivation (LNCaP-abl). CLDN3 silencing was associated with DNA methylation, loss of histone acetylation and H3K27 methylation, and was re-expressed by the combined treatment with the epigenetic modulators Aza and SAHA. From a functional point of view, CLDN3 loss was associated with increased cellular invasion. Immunohistochemical analysis showed decreased CLDN3 expression in samples from CRPC patients. Interestingly, CLDN3 expression was significantly decreased in samples from patients with high total Gleason score (≥8) and locally advanced tumors. Finally, CLDN3 loss of expression was associated with worse disease-free survival and time to clinical progression. In conclusion, our findings strongly indicate that epigenetic silencing of CLDN3 is a common event in CRPC that could be useful as a molecular marker for the prognosis of prostate cancer patients and to discriminate aggressive from indolent prostate tumors.
Asunto(s)
Neoplasias de la Próstata Resistentes a la Castración , Masculino , Humanos , Neoplasias de la Próstata Resistentes a la Castración/tratamiento farmacológico , Claudina-3/genética , Antagonistas de Andrógenos/uso terapéutico , Andrógenos/uso terapéutico , Pronóstico , Receptores Androgénicos/metabolismo , Línea Celular TumoralRESUMEN
The purpose of this work is reviewing some reduction results to deal with systems of nonautonomous ordinary differential equations with two time scales. They could be included among the so-called approximate aggregation methods. The existence of different time scales in a system, together with some long-term features, are used to build up a simpler system governed by a lesser number of state variables. The asymptotic behavior of the latter system is then used to describe the asymptotic behaviour of the former one. The reduction results are stated in two particular but important cases: periodic systems and asymptotically autonomous systems. The reduction results are illustrated with the help of simple spatial SIS epidemic models including either periodic or asymptotically autonomous terms.
Asunto(s)
Modelos Teóricos , Dinámica PoblacionalRESUMEN
In Nature, species coexistence is much more frequent than what the classical competition model predicts, so that scientists look for mechanisms that explain such a coexistence. We revisit the classical competition model assuming that individuals invest time in competing individuals of the other species. This assumption extends the classical competition model (that becomes a particular case of the model presented) under the form of a Holling type II term, that we call competitive response to interfering time. The resulting model expands the outcomes allowed by the classical model by (i) enlarging the range of parameter values that allow coexistence scenarios and (ii) displaying dynamical scenarios not allowed by the classical model: namely, bi-stable conditional coexistence in favour of i (either species coexist or species i wins) or tri-stable conditional coexistence (either species coexist or any of them goes extinct), being exclusion in both cases due to priority effects.