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Carlo M. Croce

Researcher at Ohio State University

Publications -  1156
Citations -  199822

Carlo M. Croce is an academic researcher from Ohio State University. The author has contributed to research in topics: microRNA & Cancer. The author has an hindex of 198, co-authored 1135 publications receiving 189007 citations. Previous affiliations of Carlo M. Croce include University of Nebraska Medical Center & University of California, Los Angeles.

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Involvement of BCL-2 in glucocorticoid-induced apoptosis of human pre-B-leukemias.

TL;DR: It is suggested that BCL-2 blocks the glucocorticoid-induced apoptosis of the 380 pre-B-lymphocytes by extending their survival when the level of c-myc expression is repressed.
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MicroRNAs play a central role in molecular dysfunctions linking inflammation with cancer.

TL;DR: How the factors encoded by transcripts targeted by these five miRNAs, be they transcription factors, tumor‐suppressors, or regulators of different signaling pathways, can deregulate the immune response and favor pro‐tumor immunity is focused on.
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CpG island hypermethylation-associated silencing of non-coding RNAs transcribed from ultraconserved regions in human cancer

TL;DR: The finding that, in addition to microRNAs, another class of ncRNAs (T-UCRs) undergoes DNA methylation-associated inactivation in transformed cells supports a model in which epigenetic and genetic alterations in coding and non-coding sequences cooperate in human tumorigenesis.
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PP2A-activating drugs selectively eradicate TKI-resistant chronic myeloid leukemic stem cells

TL;DR: It is shown that persistence of leukemic HSCs in BM requires inhibition of the tumor suppressor protein phosphatase 2A (PP2A) and expression--but not activity--of the BCR-ABL1 oncogene, and Targeting the JAK2/ PP2A/β-catenin network in quiescent H SCs with PADs has the potential to treat TKI-refractory CML and relieve lifelong patient dependence on
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Karyotype-specific microRNA signature in chronic lymphocytic leukemia.

TL;DR: The use of the microRNA-based classifications may yield clinically useful biomarkers of tumor behavior in CLL, and IGHV unmutated, high expression of ZAP-70 protein, and low expression of themiR-223, miR-29c, mi R-29b, and miR -181 family were strongly associated with disease progression in Cll cases harboring 17p deletion.