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Madan G. Luthra

Researcher at University of Texas MD Anderson Cancer Center

Publications -  12
Citations -  881

Madan G. Luthra is an academic researcher from University of Texas MD Anderson Cancer Center. The author has contributed to research in topics: Cancer & Gene. The author has an hindex of 9, co-authored 12 publications receiving 828 citations. Previous affiliations of Madan G. Luthra include University of Texas Health Science Center at Houston.

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MicroRNA-196a targets annexin A1: a microRNA-mediated mechanism of annexin A1 downregulation in cancers

TL;DR: A novel mechanism of post-transcriptional regulation of ANXA1 expression is demonstrated and miR-196a is identified as a marker of esophageal cancer and suggested its oncogenic potential.
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Gene Expression Profiling of Localized Esophageal Carcinomas: Association With Pathologic Response to Preoperative Chemoradiation

TL;DR: Encouraging, albeit preliminary, data suggest that expression profiling may distinguish cancers with different pathologic outcome, and is the first report to show subtypes of esophageal cancers with distinct molecular signatures.
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Correlation of mutation profile and response in patients with myelofibrosis treated with ruxolitinib

TL;DR: Target next-generation sequencing of a panel of 28 genes recurrently mutated in hematologic malignancies in a cohort of patients with myelofibrosis found that multigene profiling may be useful for therapeutic planning for MF, and patients with ≥3 mutations had the worst outcomes.
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MicroRNA-196a Is a Potential Marker of Progression during Barrett's Metaplasia-Dysplasia-Invasive Adenocarcinoma Sequence in Esophagus

TL;DR: This study evaluated the correlation of miR-196a with its in silico-predicted targets, keratin 5 (KRT5), small proline-rich protein 2C (SPRR2C), and S100 calcium-binding protein A9 (S100A9), which are down-regulated during BE progression.
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Decreased expression of gene cluster at chromosome 1q21 defines molecular subgroups of chemoradiotherapy response in esophageal cancers

TL;DR: The expression levels of genes mapping within and close to the EDC define CTXRT response subgroups in EACs, and patients in sub group I had longer survival than those in subgroup II, although this result was not statistically significant owing to the small study number.