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Alan Simmons

Researcher at University of Kentucky

Publications -  17
Citations -  692

Alan Simmons is an academic researcher from University of Kentucky. The author has contributed to research in topics: Biology & Cancer. The author has an hindex of 5, co-authored 7 publications receiving 598 citations. Previous affiliations of Alan Simmons include University of Louisville.

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Small-molecule inhibition of 6-phosphofructo-2-kinase activity suppresses glycolytic flux and tumor growth

TL;DR: 3PO markedly attenuates the proliferation of several human malignant hematopoietic and adenocarcinoma cell lines and is selectively cytostatic to ras-transformed human bronchial epithelial cells relative to normal human bronachial epithel cells.
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Nuclear targeting of 6-phosphofructo-2-kinase (PFKFB3) increases proliferation via cyclin-dependent kinases.

TL;DR: An unexpected role for PFKFB3 in nuclear signaling is demonstrated and it is indicated that Fru-2,6-BP may couple the activation of glucose metabolism with cell proliferation.
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Early Growth Response Genes Regulate B Cell Development, Proliferation, and Immune Response

TL;DR: There was a decrease in B lymphopoiesis in the bone marrow accompanied by a reduction in splenic immature and mature B cells as well as marginal zone B cells in the transgenic mice, which respond poorly to BCR cross-linking in vitro and T-independent and T -dependent Ags in vivo.
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The Role of MAPKs in B Cell Receptor-induced Down-regulation of Egr-1 in Immature B Lymphoma Cells

TL;DR: This study suggests that BCR signals reduce egr-1 expression by inhibiting activation of ERK and JNK, unlike the immature B lymphoma cells, which did not exhibit constitutive MAPK activation.
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Archetype tasks link intratumoral heterogeneity to plasticity and cancer hallmarks in small cell lung cancer.

TL;DR: In this paper , the authors apply an archetypal analysis to model plasticity by recasting SCLC phenotypic heterogeneity through multi-task evolutionary theory, and find that task trade-offs, in response to microenvironmental perturbations or treatment, may drive cell plasticity.