125 research outputs found
Comparing Regularized Kelvinlet Functions and the Finite Element Method for Registration of Medical Images to Sparse Organ Data
Image-guided surgery collocates patient-specific data with the physical
environment to facilitate surgical decision making in real-time. Unfortunately,
these guidance systems commonly become compromised by intraoperative
soft-tissue deformations. Nonrigid image-to-physical registration methods have
been proposed to compensate for these deformations, but intraoperative clinical
utility requires compatibility of these techniques with data sparsity and
temporal constraints in the operating room. While linear elastic finite element
models are effective in sparse data scenarios, the computation time for finite
element simulation remains a limitation to widespread deployment. This paper
proposes a registration algorithm that uses regularized Kelvinlets, which are
analytical solutions to linear elasticity in an infinite domain, to overcome
these barriers. This algorithm is demonstrated and compared to finite
element-based registration on two datasets: a phantom dataset representing
liver deformations and an in vivo dataset representing breast deformations. The
regularized Kelvinlets algorithm resulted in a significant reduction in
computation time compared to the finite element method. Accuracy as evaluated
by target registration error was comparable between both methods. Average
target registration errors were 4.6 +/- 1.0 and 3.2 +/- 0.8 mm on the liver
dataset and 5.4 +/- 1.4 and 6.4 +/- 1.5 mm on the breast dataset for the
regularized Kelvinlets and finite element method models, respectively. This
work demonstrates the generalizability of using a regularized Kelvinlets
registration algorithm on multiple soft tissue elastic organs. This method may
improve and accelerate registration for image-guided surgery applications, and
it shows the potential of using regularized Kelvinlets solutions on medical
imaging data.Comment: 17 pages, 9 figure
The inner membrane complex through development of Toxoplasma gondii and Plasmodium
Plasmodium spp. and Toxoplasma gondii are important human and veterinary pathogens. These parasites possess an unusual double membrane structure located directly below the plasma membrane named the inner membrane complex (IMC). First identified in early electron micrograph studies, huge advances in genetic manipulation of the Apicomplexa have allowed the visualization of a dynamic, highly structured cellular compartment with important roles in maintaining the structure and motility of these parasites. This review summarizes recent advances in the field and highlights the changes the IMC undergoes during the complex life cycles of the Apicomplexa
Surgical Patterns of Care in Patients with Invasive Breast Cancer Treated with Neoadjuvant Systemic Therapy and Breast Magnetic Resonance Imaging: Results of a Secondary Analysis of TBCRC 017
Neoadjuvant chemotherapy (NCT) down-stages advanced primary tumors, with magnetic resonance imaging (MRI) being the most sensitive imaging predictor of response. However, the impact of MRI evaluation on surgical treatment decisions in the neoadjuvant setting has not been well described. We report surgical patterns of care across 8 National Cancer Institute comprehensive cancer centers in women receiving both NCT and MRI to evaluate the impact of MRI findings on surgical planning
Magnetic Resonance Imaging as a Predictor of Pathologic Response in Patients Treated with Neoadjuvant Systemic Treatment for Operable Breast Cancer (TBCRC 017)
Increased pathologic complete response (pCR) rates observed with neoadjuvant chemotherapy (NCT) for some subsets of patients with invasive breast cancer has prompted interest in whether patients with pCR can be identified preoperatively and potentially spared the morbidity of surgery. This multicenter retrospective study was performed to estimate the accuracy of preoperative MRI in predicting pCR in the breast
Protein Kinase C Iota Regulates Pancreatic Acinar-to-Ductal Metaplasia
Pancreatic acinar-to-ductal metaplasia (ADM) is associated with an increased risk of pancreatic cancer and is considered a precursor of pancreatic ductal adenocarcinoma. Transgenic expression of transforming growth factor alpha (TGF-α) or K-rasG12D in mouse pancreatic epithelium induces ADM in vivo. Protein kinase C iota (PKCι) is highly expressed in human pancreatic cancer and is required for the transformed growth and tumorigenesis of pancreatic cancer cells. In this study, PKCι expression was assessed in a mouse model of K-rasG12D-induced pancreatic ADM and pancreatic cancer. The ability of K-rasG12D to induce pancreatic ADM in explant culture, and the requirement for PKCι, was investigated. PKCι is elevated in human and mouse pancreatic ADM and intraepithelial neoplastic lesions in vivo. We demonstrate that K-rasG12D is sufficient to induce pancreatic ADM in explant culture, exhibiting many of the same morphologic and biochemical alterations observed in TGF-α-induced ADM, including a dependence on Notch activation. PKCι is highly expressed in both TGF-α- and K-rasG12D-induced pancreatic ADM and inhibition of PKCι significantly reduces TGF-α- and K-rasG12D-mediated ADM. Inhibition of PKCι suppresses K-rasG12D–induced MMP-7 expression and Notch activation, and exogenous MMP-7 restores K-rasG12D–mediated ADM in PKCι-depleted cells, implicating a K-rasG12D-PKCι-MMP-7 signaling axis that likely induces ADM through Notch activation. Our results indicate that PKCι is an early marker of pancreatic neoplasia and suggest that PKCι is a potential downstream target of K-rasG12D in pancreatic ductal metaplasia in vivo
Origin, composition, organization and function of the inner membrane complex of Plasmodium falciparum
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