89 results match your criteria: "University of Texas at MD Anderson Cancer Center[Affiliation]"
J Palliat Med
July 2016
1 Department of Palliative Care and Rehabilitation Medicine, University of Texas at MD Anderson Cancer Center, Houston, Texas.
Aberrant opioid use is a public health issue, which has not been adequately described in the palliative care literature. With the increasing integration of palliative care into oncologic care, palliative care clinicians are seeing patients earlier in the disease trajectory, and therefore, more outpatients with chronic pain requiring chronic opioid therapy. This may have resulted in a concomitant rise in the number of patients with aberrant opioid use.
View Article and Find Full Text PDFNeuroimage
January 2016
Department of Neurology, University of California Los Angeles, Los Angeles, CA, USA.
Brain graphs provide a useful way to computationally model the network structure of the connectome, and this has led to increasing interest in the use of graph theory to quantitate and investigate the topological characteristics of the healthy brain and brain disorders on the network level. The majority of graph theory investigations of functional connectivity have relied on the assumption of temporal stationarity. However, recent evidence increasingly suggests that functional connectivity fluctuates over the length of the scan.
View Article and Find Full Text PDFBreast Cancer Res
June 2015
Department of Experimental Radiation Oncology, University of Texas at MD Anderson Cancer Center, 1515 Holcombe Blvd., Houston, TX, 77030, USA.
Pancreas
March 2015
From the *Department of Medicine, Georgetown University, Washington, DC; †Department of Medicine, Pennsylvania State University, College of Medicine, Hershey; ‡Department of Medicine, University of Pittsburgh; §University of Pittsburgh Medical Center, Pittsburgh; Departments of ∥Biochemistry and Molecular Biology, and ¶Public Health Sciences, Pennsylvania State University, College of Medicine, Hershey, PA; and #Department of Epidemiology, University of Texas at MD Anderson Cancer Center, Houston, TX.
Objective: Cholecystokinin (CCK) and gastrin stimulate growth of pancreatic cancer through the CCK-B receptor (CCK-BR). A splice variant of the CCK-BR that results from a single nucleotide polymorphism (SNP) has been identified. Because the splice variant receptor has an extended third intracellular loop, an area involved in cell signaling and growth, we hypothesized that this genetic variant could contribute to the poor prognosis and short survival of this malignancy.
View Article and Find Full Text PDFSurgery
November 2014
Surgical Outcomes and Quality Improvement Center, Feinberg School of Medicine, Northwestern University, Evanston, IL.
Background: Most studies and national programs aggregate the different types of surgical site infections (SSIs) potentially masking and misattributing risk. Determining that risk factors for superficial, deep, and organ space SSIs are unique is essential to improve SSI rates.
Methods: This cohort study utilized data of 59,365 patients who underwent colon resection at hospitals participating in the American College of Surgeons National Surgical Quality Improvement Program from 2007 to 2009.
Pediatr Nephrol
May 2015
Section of Nephrology, The University of Texas at MD Anderson Cancer Center, 1400 Pressler Street, Unit 1468, Houston, TX, 77030, USA.
MicroRNAs (miRNAs) are short, non-coding RNAs that employ classic Watson-Crick base-pairing to identify their target genes, ultimately resulting in destabilization of their target mRNAs and/or inhibition of their translation. The role of miRNAs in a wide range of human diseases, including those afflicting the kidney, has been intensely investigated. However, there is still a vast dearth of knowledge regarding their specific mode of action and therapeutic effects in various kidney diseases.
View Article and Find Full Text PDFPigment Cell Melanoma Res
January 2014
Department of Cancer Biology, The University of Texas at MD Anderson Cancer Center, Houston, TX, USA.
Malignant melanoma is one of the most aggressive cancers and can disseminate from a relatively small primary tumor and metastasize to multiple sites, including the lung, liver, brain, bone, and lymph nodes. Elucidating the molecular and genetic changes that take place during the metastatic process has led to a better understanding of why melanoma is so metastatic. Herein, we describe the unique features that distinguish melanoma from other solid tumors and contribute to the malignant phenotype of melanoma cells.
View Article and Find Full Text PDFCrit Care Nurs Clin North Am
March 2013
The University of Texas at MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX 77030, USA.
Noninsulin antidiabetic medications coupled with diet and exercise are effective in managing most patients with type 2 diabetes. However, it is essential to evaluate the safety and effectiveness of the home antidiabetic medication regimen when the patient is hospitalized. Prescribers need to be aware of the mechanism of action of each class, contraindications, precautions, and adverse effects to formulate a safe and effective management plan.
View Article and Find Full Text PDFBiol Blood Marrow Transplant
March 2013
Department of Stem Cell Transplantation and Cellular Therapy, The University of Texas at MD Anderson Cancer Center, Houston, TX 77030, USA.
Dose intensity is important for disease control in patients undergoing allogeneic stem cell transplantation. We conducted a phase I/II controlled, adoptive, randomized study to determine the optimal dosing schedule of i.v.
View Article and Find Full Text PDFPigment Cell Melanoma Res
September 2012
Department of Cancer Biology, The University of Texas at MD Anderson Cancer Center, Houston, TX, USA.
Melanoma is the leading cause of skin cancer-related deaths, which is due in large part to its aggressive behavior, resistance to therapy, and ability to metastasize to multiple organs such as the lymph nodes, lung, and brain. Melanoma progresses in a stepwise manner from the benign nevus, to radial spreading through the dermis, to a vertical invasive phase, and finally to metastasis. The carbohydrate-binding family of galectins has a strong influence on each phase of melanoma progression through their effects on immune surveillance, angiogenesis, cell migration, tumor cell adhesion, and the cellular response to chemotherapy.
View Article and Find Full Text PDFRheum Dis Clin North Am
November 2011
Section of Rheumatology, Department of General Internal Medicine, The University of Texas at MD Anderson Cancer Center, 1515 Holcombe Boulevard, Unit 1465, Houston, TX 77030, USA.
Bone tumors can show a wide range of nonspecific rheumatic manifestations. The presence of unexplained or atypical chronic bone pain, an enlarging bone mass, neurovascular compression syndromes, or pathologic fractures should alert us to the possibility of a bone tumor causing these symptoms. These patients must undergo a complete physical examination; adequate imaging; and, if needed, a biopsy to confirm their diagnosis and offer them an opportune treatment.
View Article and Find Full Text PDFAm J Bioeth
December 2009
University of Texas at MD Anderson Cancer Center, Houston, TX 77030, USA.
Bone Marrow Transplant
April 2010
Department of Pulmonary Medicine, The University of Texas at MD Anderson Cancer Center, Houston, TX 77030, USA.
Pulmonary infiltrates frequently complicate hematopoietic SCT (HSCT). The utility of fiberoptic bronchoscopy (FOB) with bronchoalveolar lavage (BAL) in the evaluation of new pulmonary infiltrates, particularly as it relates to optimal timing of the procedure, is unclear. Based on this, we retrospectively reviewed 501 consecutive, adult, nonintubated patients who underwent 598 BALs for evaluation of new pulmonary infiltrates during the first 100 days following HSCT to determine whether diagnostic yields for infection, subsequent antimicrobial treatment modifications and patient outcomes differed following early vs late referrals for the procedure.
View Article and Find Full Text PDFCurr Opin Gastroenterol
January 2002
The University of Texas at MD Anderson Cancer Center, Houston, Texas 77030, USA.
Malignant transformation is now known to require a series of molecular alterations that disrupt a limited number of pathways including autocrine and paracrine responses to growth factors, cell-cycle control, senescence, motility, and invasion. Studies on hereditary cancers have established genetic changes as the primary driving force for these molecular alterations. Recently, however, it has been recognized that epigenetic changes, defined as clonal changes in gene expression without accompanying changes in primary DNA coding sequence, can also be a driving force in neoplastic transformation, for selected genes, and in specific tumors.
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