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Dive into the research topics where Jahan J. Mohiuddin is active.

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Featured researches published by Jahan J. Mohiuddin.


Cancer | 2016

Use of stereotactic body radiotherapy for prostate cancer in the United States from 2004 through 2012

Brock R. Baker; Ramsankar Basak; Jahan J. Mohiuddin; Ronald C. Chen

Stereotactic body radiotherapy (SBRT) is a newer treatment option for patients with localized prostate cancer. The rates of diffusion of this technology across the United States are unknown. The goal of the current study was to describe the use of SBRT among patients with prostate cancer based on different risk groups (low, intermediate, or high risk) and by type of facility (community cancer program, comprehensive community cancer program, or academic program) in which patients were treated.


Nature Reviews Urology | 2015

Radiotherapy for high-risk prostate cancer

Jahan J. Mohiuddin; Brock R. Baker; Ronald C. Chen

The combination of radiation treatment and long-term androgen deprivation therapy (ADT) has been shown in multiple clinical trials to prolong overall survival in men with high-risk prostate cancer compared with either treatment alone. New radiation technologies enable the safe delivery of high radiation doses that improve cancer control compared with lower radiation doses. Based on the results of multiple randomized trials, clinical practice guidelines for high-risk prostate cancer recommend total radiation doses of at least 75.6 Gy, with long-term (2–3 years) ADT. Ongoing research into hypofractionated radiation treatment, whole-pelvic radiation, and combinations of radiation with novel hormonal agents could further improve cancer control and survival outcomes for patients with high-risk prostate cancer.


Journal of Molecular Biology | 2013

Structure and function of palladin's actin binding domain.

Moriah R. Beck; Richard D. S. Dixon; Silvia M. Goicoechea; Grant S. Murphy; Joseph G. Brungardt; Matthew T. Beam; Pavan Srinath; Julie Patel; Jahan J. Mohiuddin; Carol A. Otey; Sharon L. Campbell

Here, we report the NMR structure of the actin-binding domain contained in the cell adhesion protein palladin. Previously, we demonstrated that one of the immunoglobulin domains of palladin (Ig3) is both necessary and sufficient for direct filamentous actin binding in vitro. In this study, we identify two basic patches on opposite faces of Ig3 that are critical for actin binding and cross-linking. Sedimentation equilibrium assays indicate that the Ig3 domain of palladin does not self-associate. These combined data are consistent with an actin cross-linking mechanism that involves concurrent attachment of two actin filaments by a single palladin molecule by an electrostatic mechanism. Palladin mutations that disrupt actin binding show altered cellular distributions and morphology of actin in cells, revealing a functional requirement for the interaction between palladin and actin in vivo.


Cancer | 2016

Evaluation of the effectiveness of adding androgen deprivation to modern dose-escalated radiotherapy for men with favorable intermediate-risk prostate cancer.

Aaron D. Falchook; Ramsankar Basak; Jahan J. Mohiuddin; Ronald C. Chen

Randomized trials have shown that androgen‐deprivation therapy (ADT) improves survival for men with intermediate‐risk prostate cancer treated with radiotherapy (RT). The benefit of ADT to patients with favorable intermediate‐risk prostate cancer treated with modern dose‐escalated RT is unknown. This study evaluated the effectiveness of ADT on survival of men with favorable intermediate‐risk prostate cancer treated with dose‐escalated RT.


JNCI Cancer Spectrum | 2017

Evaluating the Effectiveness of Neoadjuvant Chemotherapy in Reducing Mastectomy for Women With Breast Cancer

Jahan J. Mohiuddin; Allison M. Deal; Jennifer L. Lund; Lisa A. Carey; Brock R. Baker; Timothy M. Zagar; Ellen L. Jones; Lawrence B. Marks; Ronald C. Chen

Abstract Background Neoadjuvant chemotherapy in breast cancer reduced mastectomy rates by 7% to 13% in randomized trials. However, the differential effects for women with different stages, receptor subtypes, and ages are unknown. We compared mastectomy rates in women who did vs did not receive neoadjuvant chemotherapy in 18 patient subgroups. The main objective was to quantify the potential benefit from neoadjuvant chemotherapy in reducing mastectomy rates for each subgroup. Methods Our retrospective analysis used data from the National Cancer Data Base, which includes approximately 70% of incident cancers across the United States. Absolute risk reductions for mastectomy were determined for 18 subgroups of clinical stage, receptor subtype, and age group. In each subgroup, propensity score weighting balanced measured covariates between women treated with vs without neoadjuvant chemotherapy. Results A total of 55 709 patients were analyzed. In clinical stage IIA disease, only patients with human epidermal growth factor receptor 2 (HER2)–positive tumors had reduced mastectomy rates associated with neoadjuvant chemotherapy (age < 60 years, 12%; age ≥ 60 years, 12.6%). For stage IIB cancers, neoadjuvant chemotherapy was associated with an absolute reduction in mastectomy rates of 5.9% in women younger than age 60 years with hormone receptor–positive/HER2- disease, 8.2% to 10.7% for triple-negative disease, and 11.7% to 17.4% for HER2+ disease. For stage IIIA, the reductions in mastectomy rates ranged from 6.6% to 15.9%. Conclusions In an analysis of patients treated across the United States, we found that neoadjuvant chemotherapy was associated with a reduction in mastectomy rates to a similar magnitude overall as shown in randomized trials, but this benefit varied widely by patient subgroup. This study provides novel information to help women make informed decisions regarding treatment.


Prostate Cancer (Second Edition)#R##N#Science and Clinical Practice | 2016

Radiation with Hormonal Therapy

Brock R. Baker; Jahan J. Mohiuddin; Ronald C. Chen

External beam radiation therapy (EBRT) is an effective primary treatment for patients with nonmetastatic prostate cancer, and is often used together with androgen deprivation therapy (ADT) in patients with aggressive (intermediate- or high-risk) disease. A large number of randomized trials have been conducted over the past 40 years, which guide clinical practice today. This chapter summarizes results of these trials and other key literature related to the use of EBRT and ADT, as well as potential side effects of treatment and their management.


American Journal of Physiology-gastrointestinal and Liver Physiology | 2013

Paneth cells expand from newly created and preexisting cells during repair after doxorubicin-induced damage

Stephanie L. King; Jahan J. Mohiuddin; Christopher M. Dekaney


Oncology | 2015

The role of radiotherapy in node-positive prostate cancer.

Brock R. Baker; Jahan J. Mohiuddin; Ronald C. Chen


JAMA Oncology | 2016

Use of Androgen Deprivation Therapy With Radiotherapy for Intermediate- and High-Risk Prostate Cancer Across the United States.

Aaron D. Falchook; Ramsankar Basak; Jahan J. Mohiuddin; Ronald C. Chen


Journal of The American College of Surgeons | 2016

Neoadjuvant Systemic Therapy Use for Younger Patients with Breast Cancer Treated in Different Types of Cancer Centers Across the United States.

Jahan J. Mohiuddin; Allison M. Deal; Lisa A. Carey; Jennifer L. Lund; Brock R. Baker; Timothy M. Zagar; Ellen L. Jones; Lawrence B. Marks; Ronald C. Chen

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Ronald C. Chen

University of North Carolina at Chapel Hill

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Brock R. Baker

University of North Carolina at Chapel Hill

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Allison M. Deal

University of North Carolina at Chapel Hill

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Lisa A. Carey

University of North Carolina at Chapel Hill

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Aaron D. Falchook

University of North Carolina at Chapel Hill

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Ellen L. Jones

University of North Carolina at Chapel Hill

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Jennifer L. Lund

University of North Carolina at Chapel Hill

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Lawrence B. Marks

University of North Carolina at Chapel Hill

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Ramsankar Basak

University of North Carolina at Chapel Hill

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Timothy M. Zagar

University of North Carolina at Chapel Hill

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