Automatic detection of liver tumor motion by fluoroscopy images

Background: A method to track liver tumor motion signals from fluoroscopic images without any implanted gold fiducial markers was proposed in this study to overcome the adverse effects on precise tumor irradiation caused by respiratory movement

Materials and Methods: The method was based on the following idea: [i] Before treatment, a series of fluoroscopic images corresponding to different breathing phases and tumor positions were acquired after patient set-up; [iii] The wavelet transform method and Canny edge detection algorithm were used to detect motion trajectory of the diaphragm; [iv] The motion curves of center of lipiodol in the images were obtained by mathematical morphology and median filtering algorithm. The method was evaluated using by five sequences of fluoroscopic images from TACE patients who received transcatheter arterial chemoembolization therapy

Results: The position of liver tumor was significantly affected by respiratory motion; the motion trajectories of the diaphragm and lipiodolagreed well with the manually marked locations in amplitude and period; the motion trajectories of the diaphragm and lipiodol almost had similar period and amplitude in one treatment fraction. The respiratory period and amplitude of the same patient in different fractions had no significant differences; however, the difference was obvious for different patients. The proposed lipiodol detection methods can effectively reflect the relevant rules of tumor location caused by respiratory movement

Conclusion: Direct tracking of liver tumor motion in fluoroscopic images is feasible. The automatic detection method can reflect the characteristics of respiratory and tumor motions, which can save much time and significantly improve measurement precision compared with manual measurement

Analysis of Structures, Functions, and Epitopes of Aminopeptidase from Trichinella spiralis

We have previously reported that the recombinant T. spiralis aminopeptidase (rTsAP) could induce a partial protective immunity against T. spiralis infection in mice. The aim of this study was to predict the structures and functions of TsAP protein by using the full length cDNA sequence of TsAP gene. TsAP sequence was 1515 bp length with a 1515 bp biggest ORF encoding 504-amino acid protein. The molecular weight and isoelectric point of TsAP were 54.7 kDa and 6.69, respectively. TsAP structure domains contained a Peptidase_M17_N and a Peptidase_M17 domain, which has the function of catalysis of the hydrolysis of N-terminal amino acid residues. TsAP had no signal peptide site and transmembrane domain, and located in cytoplasm. The secondary structure of TsAP contained 16 α-helix, 14 β-strand and 29 coils. The TsAP had 11 and 21 potential antigenic epitopes of T cell and B cell, respectively. Based on the phylogenetic analyses of TsAP, T. spiralis have the closest relationship with Plasmodium falciparum. TsAP was a kind of proteolytic enzyme with a variety of biological functions and its antigenic epitopes could provide important insights on the diagnostic antigens and target molecular of anti-Trichinella drugs