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Alexandra Giatromanolaki

Researcher at Democritus University of Thrace

Publications -  360
Citations -  26647

Alexandra Giatromanolaki is an academic researcher from Democritus University of Thrace. The author has contributed to research in topics: Angiogenesis & Cancer. The author has an hindex of 66, co-authored 340 publications receiving 22956 citations. Previous affiliations of Alexandra Giatromanolaki include John Radcliffe Hospital.

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Loss of expression and nuclear/cytoplasmic localization of the FOXP1 forkhead transcription factor are common events in early endometrial cancer: relationship with estrogen receptors and HIF-1alpha expression.

TL;DR: Evidence on pathways to be investigated to elucidate the interplay between FOXP1, ER-α and HIF-1α in hormone dependent cancers is provided and survival analysis did not reveal significant differences among patients grouped by FoxP1 expression.
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Hypoxia-activated tumor pathways of angiogenesis and pH regulation independent of anemia in head-and-neck cancer.

TL;DR: Targeting the hypoxia-regulated molecular cascade emerged as a complementary radiosensitization strategy for a large group of patients with hypoxic tumors, who are unlikely to benefit from conventional approaches aiming to improve intratumoral oxygen delivery through anemia correction.
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Autophagy patterns and prognosis in uveal melanomas.

TL;DR: It is concluded that autophagy is commonly upregulated in uveal melanomas, and may be associated with hypoxia and intense pigmentation, and there is a strong association between extensive BECN1 overexpression and early metastases/poor prognosis, and between underexpression of this protein and late metastases and better prognosis.
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Fever-range hyperthermia vs. hypothermia effect on cancer cell viability, proliferation and HSP90 expression

TL;DR: Of interest, mild hypothermia had a universal suppressing effect on cancer cell proliferation, further supporting the radio-sensitization hypothesis through reduction of oxygen and metabolic demands.
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The pathology of tumor stromatogenesis.

TL;DR: Cancer cells and neostroma should not be seen as a mixture of heterogeneous uncoordinated cells but rather as a unified morphologic and metabolic domain with a harmonious collaboration between aerobic (myofibroblasts, endothelial cells) and anaerobic compartments (cancer cells).