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1.
Acta Oncol ; 61(1): 14-21, 2022 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-34694198

RESUMEN

BACKGROUND: Ulceration is an independent adverse prognostic factor in cutaneous malignant melanoma (CMM). There is, however, a need for additional prognostic markers to identify patients with ulcerated stage I-II CMM who have a high-risk for recurrence. The aim of this study was to examine the prognostic impact of BRAF mutation, proliferation and presence of tumour infiltrating lymphocytes (TILs) in primary ulcerated CMM. MATERIAL AND METHODS: We have used a consecutive cohort consisting of 71 primary ulcerated CMM (T1b-T4b). BRAF mutation was detected using Cobas test and pyrosequencing. Protein expression of the proliferation marker Ki67 was analysed using immunohistochemistry. Presence of TILs was evaluated in representative hematoxylin-eosin stained formalin-fixed paraffin-embedded tumour sections. RESULTS: Proportion of BRAF mutated alleles, proliferation and presence of TILs all had a statistically significant impact on recurrence free survival in univariate analyses (HR 2.44, 95% CI 1.23-4.84, p = 0.011; HR 2.66, 95% CI 1.32-5.35, p = 0.006 respectively HR 0.48, 95% CI 0.24-0.98, p = 0.045). A trend test found a statistically significant decrease in the proportion of recurrence by including the three favourable factors (BRAF wildtype/low proportion of BRAF mutated alleles, low proliferation and high presence of TILs) (p = 0.0004). When at least two out of three factors were present there was a statistically significant association with longer recurrence free survival in the multivariate analysis (HR 0.30, 95% CI 0.15-0.61, p = 0.001) when adjusted for Breslow thickness, an established independent prognostic marker for CMM. CONCLUSION: Thus, this panel of markers could be an interesting novel concept for predicting the clinical outcome in patients with high-risk stage I-II ulcerated CMM.


Asunto(s)
Melanoma , Neoplasias Cutáneas , Humanos , Linfocitos Infiltrantes de Tumor , Melanoma/genética , Pronóstico , Neoplasias Cutáneas/genética , Úlcera
2.
Plant Physiol ; 139(4): 1635-48, 2005 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-16299183

RESUMEN

We have studied autumn leaf senescence in a free-growing aspen (Populus tremula) by following changes in pigment, metabolite and nutrient content, photosynthesis, and cell and organelle integrity. The senescence process started on September 11, 2003, apparently initiated solely by the photoperiod, and progressed steadily without any obvious influence of other environmental signals. For example, after this date, senescing leaves accumulated anthocyanins in response to conditions inducing photooxidative stress, but at the beginning of September the leaves did not. Degradation of leaf constituents took place over an 18-d period, and, although the cells in each leaf did not all senesce in parallel, senescence in the tree as a whole was synchronous. Lutein and beta-carotene were degraded in parallel with chlorophyll, whereas neoxanthin and the xanthophyll cycle pigments were retained longer. Chloroplasts in each cell were rapidly converted to gerontoplasts and many, although not all, cells died. From September 19, when chlorophyll levels had dropped by 50%, mitochondrial respiration provided the energy for nutrient remobilization. Remobilization seemed to stop on September 29, probably due to the cessation of phloem transport, but, up to abscission of the last leaves (over 1 week later), some cells were metabolically active and had chlorophyll-containing gerontoplasts. About 80% of the nitrogen and phosphorus was remobilized, and on September 29 a sudden change occurred in the delta15N of the cellular content, indicating that volatile compounds may have been released.


Asunto(s)
Hojas de la Planta/crecimiento & desarrollo , Populus/crecimiento & desarrollo , Estaciones del Año , Antocianinas/metabolismo , Carotenoides/metabolismo , Clorofila/metabolismo , Cloroplastos/metabolismo , Microscopía Electrónica , Mitocondrias/metabolismo , Nitrógeno/metabolismo , Fósforo/metabolismo , Fotobiología , Fotoperiodo , Fotosíntesis , Pigmentos Biológicos/metabolismo , Hojas de la Planta/citología , Hojas de la Planta/metabolismo , Populus/citología , Populus/metabolismo
3.
Genome Biol ; 5(4): R24, 2004.
Artículo en Inglés | MEDLINE | ID: mdl-15059257

RESUMEN

BACKGROUND: We have developed genomic tools to allow the genus Populus (aspens and cottonwoods) to be exploited as a full-featured model for investigating fundamental aspects of tree biology. We have undertaken large-scale expressed sequence tag (EST) sequencing programs and created Populus microarrays with significant gene coverage. One of the important aspects of plant biology that cannot be studied in annual plants is the gene activity involved in the induction of autumn leaf senescence. RESULTS: On the basis of 36,354 Populus ESTs, obtained from seven cDNA libraries, we have created a DNA microarray consisting of 13,490 clones, spotted in duplicate. Of these clones, 12,376 (92%) were confirmed by resequencing and all sequences were annotated and functionally classified. Here we have used the microarray to study transcript abundance in leaves of a free-growing aspen tree (Populus tremula) in northern Sweden during natural autumn senescence. Of the 13,490 spotted clones, 3,792 represented genes with significant expression in all leaf samples from the seven studied dates. CONCLUSIONS: We observed a major shift in gene expression, coinciding with massive chlorophyll degradation, that reflected a shift from photosynthetic competence to energy generation by mitochondrial respiration, oxidation of fatty acids and nutrient mobilization. Autumn senescence had much in common with senescence in annual plants; for example many proteases were induced. We also found evidence for increased transcriptional activity before the appearance of visible signs of senescence, presumably preparing the leaf for degradation of its components.


Asunto(s)
Envejecimiento/genética , Fenómenos Cronobiológicos/genética , Estaciones del Año , Transcripción Genética/genética , Muerte Celular/genética , ADN Complementario/genética , ADN de Plantas/genética , Etiquetas de Secuencia Expresada , Perfilación de la Expresión Génica/métodos , Regulación de la Expresión Génica de las Plantas/genética , Biblioteca de Genes , Análisis de Secuencia por Matrices de Oligonucleótidos/métodos , Hojas de la Planta/genética , Populus/citología , Populus/genética , ARN de Planta/genética , Análisis de Secuencia de ADN/métodos
4.
Plant Physiol ; 131(2): 430-42, 2003 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-12586868

RESUMEN

Two cDNA libraries were prepared, one from leaves of a field-grown aspen (Populus tremula) tree, harvested just before any visible sign of leaf senescence in the autumn, and one from young but fully expanded leaves of greenhouse-grown aspen (Populus tremula x tremuloides). Expressed sequence tags (ESTs; 5,128 and 4,841, respectively) were obtained from the two libraries. A semiautomatic method of annotation and functional classification of the ESTs, according to a modified Munich Institute of Protein Sequences classification scheme, was developed, utilizing information from three different databases. The patterns of gene expression in the two libraries were strikingly different. In the autumn leaf library, ESTs encoding metallothionein, early light-inducible proteins, and cysteine proteases were most abundant. Clones encoding other proteases and proteins involved in respiration and breakdown of lipids and pigments, as well as stress-related genes, were also well represented. We identified homologs to many known senescence-associated genes, as well as seven different genes encoding cysteine proteases, two encoding aspartic proteases, five encoding metallothioneins, and 35 additional genes that were up-regulated in autumn leaves. We also indirectly estimated the rate of plastid protein synthesis in the autumn leaves to be less that 10% of that in young leaves.


Asunto(s)
Regulación de la Expresión Génica de las Plantas/genética , Hojas de la Planta/genética , Estaciones del Año , Proteínas de Arabidopsis , Ácido Aspártico Endopeptidasas/genética , Ácido Aspártico Endopeptidasas/metabolismo , Respiración de la Célula/genética , Respiración de la Célula/fisiología , Biología Computacional , Cisteína Endopeptidasas/genética , Cisteína Endopeptidasas/metabolismo , Bases de Datos Genéticas , Etiquetas de Secuencia Expresada , Perfilación de la Expresión Génica/métodos , Metabolismo de los Lípidos , Metalotioneína/genética , Metalotioneína/metabolismo , Fotosíntesis/genética , Hojas de la Planta/crecimiento & desarrollo , Proteínas de Plantas/genética , Proteínas de Plantas/metabolismo , Populus/genética , Populus/crecimiento & desarrollo , ARN de Planta/genética , ARN de Planta/metabolismo
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