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1.
Head Neck ; 46(4): 896-904, 2024 04.
Artículo en Inglés | MEDLINE | ID: mdl-38216834

RESUMEN

BACKGROUND: Massive oropharyngeal bleeding post-chemoradiotherapy is a life-threatening condition that requires emergent management. METHODS: This retrospective case series included 11 patients with oropharyngeal squamous cell carcinoma who suffered from massive bleeding during or following treatment with definitive chemoradiotherapy. Details of acute and definitive management of oropharyngeal bleeding are reported. RESULTS: Nine of 11 hemorrhagic events occurred a mean (SD) of 88.6 days (53.6) after radiotherapy. Airway intubation and embolization were performed in 10 of 11 patients, followed by surgery in 7 of 11 patients. The most commonly embolized vessels were the external carotid and lingual arteries. At the time of discharge, 3 of 11 patients had a tracheostomy, and 7 of 11 continued to use a gastrostomy tube. Four patients died. CONCLUSIONS: Hemorrhagic complications in oropharyngeal cancer treatment require emergent responses. Developing a workflow for coordination between multidisciplinary teams can maximize probability of survival and decrease morbidity.


Asunto(s)
Carcinoma de Células Escamosas , Neoplasias Orofaríngeas , Humanos , Estudios Retrospectivos , Neoplasias Orofaríngeas/complicaciones , Neoplasias Orofaríngeas/terapia , Neoplasias Orofaríngeas/patología , Hemorragia/etiología , Hemorragia/terapia , Quimioradioterapia/efectos adversos , Carcinoma de Células Escamosas/complicaciones , Carcinoma de Células Escamosas/terapia
2.
J Cell Biol ; 218(1): 171-189, 2019 01 07.
Artículo en Inglés | MEDLINE | ID: mdl-30459262

RESUMEN

In many cells, morphogenetic events are coordinated with the cell cycle by cyclin-dependent kinases (CDKs). For example, many mammalian cells display extended morphologies during interphase but round up into more spherical shapes during mitosis (high CDK activity) and constrict a furrow during cytokinesis (low CDK activity). In the budding yeast Saccharomyces cerevisiae, bud formation reproducibly initiates near the G1/S transition and requires activation of CDKs at a point called "start" in G1. Previous work suggested that CDKs acted by controlling the ability of cells to polarize Cdc42, a conserved Rho-family GTPase that regulates cell polarity and the actin cytoskeleton in many systems. However, we report that yeast daughter cells can polarize Cdc42 before CDK activation at start. This polarization operates via a positive feedback loop mediated by the Cdc42 effector Ste20. We further identify a major and novel locus of CDK action downstream of Cdc42 polarization, affecting the ability of several other Cdc42 effectors to localize to the polarity site.


Asunto(s)
Polaridad Celular/genética , Puntos de Control de la Fase G1 del Ciclo Celular/genética , Regulación Fúngica de la Expresión Génica , Quinasas Quinasa Quinasa PAM/genética , Proteínas de Saccharomyces cerevisiae/genética , Saccharomyces cerevisiae/genética , Proteína de Unión al GTP cdc42 de Saccharomyces cerevisiae/genética , Citoesqueleto de Actina/metabolismo , Citoesqueleto de Actina/ultraestructura , Citocinesis/genética , Retroalimentación Fisiológica , Quinasas Quinasa Quinasa PAM/metabolismo , Mitosis/genética , Saccharomyces cerevisiae/metabolismo , Saccharomyces cerevisiae/ultraestructura , Proteínas de Saccharomyces cerevisiae/metabolismo , Transducción de Señal , Factores de Tiempo , Proteína de Unión al GTP cdc42 de Saccharomyces cerevisiae/metabolismo
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