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Leila R. Martins

Researcher at Instituto de Medicina Molecular

Publications -  20
Citations -  1247

Leila R. Martins is an academic researcher from Instituto de Medicina Molecular. The author has contributed to research in topics: Leukemia & PI3K/AKT/mTOR pathway. The author has an hindex of 13, co-authored 17 publications receiving 1128 citations. Previous affiliations of Leila R. Martins include German Cancer Research Center & University of Lisbon.

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PTEN posttranslational inactivation and hyperactivation of the PI3K/Akt pathway sustain primary T cell leukemia viability.

TL;DR: Overall, the data indicate that T-ALL cells inactivate PTEN mostly in a nondeletional, posttranslational manner, and Pharmacological manipulation of these mechanisms may open new avenues for T-all treatment.
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Low doses of ionizing radiation promote tumor growth and metastasis by enhancing angiogenesis.

TL;DR: It is shown that low-dose IR promotes tumor growth and metastasis and that these effects were prevented by the administration of a VEGF receptor-tyrosine kinase inhibitor immediately before IR exposure, demonstrating a new mechanism to the understanding of the potential pro-metastatic effect of IR.
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IL-7 Contributes to the Progression of Human T-cell Acute Lymphoblastic Leukemias

TL;DR: It is established that interleukin-7 contributes to the progression of human T-cell leukemia, and the results offer preclinical validation of the concept that targeting IL-7/IL-7R signaling in the tumor microenvironment could elicit therapeutic effects in T-ALL.
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Adult B-cell acute lymphoblastic leukemia cells display decreased PTEN activity and constitutive hyperactivation of PI3K/Akt pathway despite high PTEN protein levels

TL;DR: It is found that adult B-cell acute lymphoblastic leukemia samples show significantly higher CK2 kinase activity and lower PTEN lipid phosphatase activity than healthy controls, and it is suggested that CK2 inhibition may constitute a valid, novel therapeutic tool in this malignancy.
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Activity of the clinical-stage CK2-specific inhibitor CX-4945 against chronic lymphocytic leukemia

TL;DR: Activity of the clinical-stage CK2-specific inhibitor CX-4945 against chronic lymphocytic leukemia is inhibited by a second substance called CK2A, which is cytotoxic to lymphocytes and excites the immune system to attack these cells.