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Article ; Online: Phosphorylation of the F-BAR protein Hof1 drives septin ring splitting in budding yeast.

Varela Salgado, Maritzaida / Adriaans, Ingrid E / Touati, Sandra A / Ibanes, Sandy / Lai-Kee-Him, Joséphine / Ancelin, Aurélie / Cipelletti, Luca / Picas, Laura / Piatti, Simonetta

Nature communications

2024 Volume 15, Issue 1, Page(s) 3383

Abstract: ... essential for cytokinesis. However, the effectors of MEN in this process are unknown. Here we identify the F ... requires its F-BAR domain, suggesting that it may involve a local membrane remodelling that leads to septin ...

Abstract	A double septin ring accompanies cytokinesis in yeasts and mammalian cells. In budding yeast, reorganisation of the septin collar at the bud neck into a dynamic double ring is essential for actomyosin ring constriction and cytokinesis. Septin reorganisation requires the Mitotic Exit Network (MEN), a kinase cascade essential for cytokinesis. However, the effectors of MEN in this process are unknown. Here we identify the F-BAR protein Hof1 as a critical target of MEN in septin remodelling. Phospho-mimicking HOF1 mutant alleles overcome the inability of MEN mutants to undergo septin reorganisation by decreasing Hof1 binding to septins and facilitating its translocation to the actomyosin ring. Hof1-mediated septin rearrangement requires its F-BAR domain, suggesting that it may involve a local membrane remodelling that leads to septin reorganisation. In vitro Hof1 can induce the formation of intertwined septin bundles, while a phosphomimetic Hof1 protein has impaired septin-bundling activity. Altogether, our data indicate that Hof1 modulates septin architecture in distinct ways depending on its phosphorylation status.
MeSH term(s)	Saccharomyces cerevisiae Proteins/metabolism ; Saccharomyces cerevisiae Proteins/genetics ; Phosphorylation ; Septins/metabolism ; Septins/genetics ; Saccharomyces cerevisiae/metabolism ; Saccharomyces cerevisiae/genetics ; Cytokinesis ; Cell Cycle Proteins/metabolism ; Cell Cycle Proteins/genetics ; Actomyosin/metabolism ; Saccharomycetales/metabolism ; Saccharomycetales/genetics ; Mutation ; Protein Binding ; Microtubule-Associated Proteins
Chemical Substances	Saccharomyces cerevisiae Proteins ; Septins (EC 3.6.1.-) ; HOF1 protein, S cerevisiae ; Cell Cycle Proteins ; Actomyosin (9013-26-7) ; Microtubule-Associated Proteins
Language	English
Publishing date	2024-04-22
Publishing country	England
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID	2553671-0
ISSN	2041-1723 ; 2041-1723
ISSN (online)	2041-1723
ISSN	2041-1723
DOI	10.1038/s41467-024-47709-3
Database	MEDical Literature Analysis and Retrieval System OnLINE

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Article ; Online: Regulation of PP1 interaction with I-2, neurabin, and F-actin.

Foley, Karl / Ward, Nancy / Hou, Hailong / Mayer, Abigail / McKee, Cody / Xia, Houhui

Molecular and cellular neurosciences

2022 Volume 124, Page(s) 103796

Abstract: ... and F-actin. Finally, we found that stabilizing F-actin promotes Nrb-PP1 binding and may also lead ... to conformational changes between Nrb-I-2 and Nrb-F-actin complexes. Overall, our findings elaborate the dynamic ...

Abstract	Reversible phosphorylation is a fundamental regulatory mechanism required for many biological processes and is coordinated by the opposing actions of protein kinases and phosphatases. Protein phosphatase 1 (PP1) is a major protein phosphatase that plays an important role in many fundamental physiological processes including synaptic transmission and memory formation. Here we investigate the regulation of PP1 by prominent signaling proteins and synaptic scaffolds including GSK3β, inhibitor-2 (I-2), neurabin (Nrb), and actin. While GSK3β is known to regulate PP1 via phosphorylation of the PP1-binding protein I-2, we found that GSK3β directly regulates PP1 via inhibitory phosphorylation in neurons. Additionally, using bioluminescence resonance energy transfer (BRET), we found that GSK3β alters PP1-I-2 interaction in living cells. The effect of GSK3β on PP1-I-2 interaction is independent of the PP1 C-terminal tail, contrary to predictions based on previous findings from purified proteins. I-2 has been shown to form a trimeric complex with PP1 and Nrb, a major synaptic scaffold for promoting PP1 localization to the actin cytoskeleton. Utilizing BRET, we found that Nrb promotes PP1-actin interaction, however no BRET was detected between I-2 and F-actin. Finally, we found that stabilizing F-actin promotes Nrb-PP1 binding and may also lead to conformational changes between Nrb-I-2 and Nrb-F-actin complexes. Overall, our findings elaborate the dynamic regulation of PP1 complexes by GSK3β, targeting proteins, and actin polymerization.
MeSH term(s)	Protein Phosphatase 1/metabolism ; Actins/metabolism ; Glycogen Synthase Kinase 3 beta/metabolism ; Actin Cytoskeleton/metabolism ; Phosphorylation
Chemical Substances	Protein Phosphatase 1 (EC 3.1.3.16) ; Actins ; neurabin ; Glycogen Synthase Kinase 3 beta (EC 2.7.11.1)
Language	English
Publishing date	2022-11-25
Publishing country	United States
Document type	Journal Article ; Research Support, N.I.H., Extramural ; Research Support, U.S. Gov't, Non-P.H.S.
ZDB-ID	1046640-x
ISSN	1095-9327 ; 1044-7431
ISSN (online)	1095-9327
ISSN	1044-7431
DOI	10.1016/j.mcn.2022.103796
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Article: [¹⁸F]THK5351 PET Imaging in Patients with Mild Cognitive Impairment.

Jeong, Hye Jin / Lee, Hyon / Lee, Sang Yoon / Seo, Seongho / Park, Kee Hyung / Lee, Yeong Bae / Shin, Dong Jin / Kang, Jae Myeong / Yeon, Byeong Kil / Kang, Seung Gul / Cho, Jaelim / Seong, Joon Kyung / Okamura, Nobuyuki / Villemagne, Victor L / Na, Duk L / Noh, Young

Journal of clinical neurology (Seoul, Korea)

2020 Volume 16, Issue 2, Page(s) 202–214

Abstract: ... the positron emission tomography (PET) tracer [¹⁸F]THK5351 in MCI subgroups.: Methods: This study included 96 participants ... who underwent 3.0-T MRI, [¹⁸F]THK5351 PET, and detailed neuropsychological tests. [¹⁸F]flutemetamol PET was also ... were performed to evaluate the retention of [¹⁸F]THK5351 in the MCI subgroups. Subgroup analysis ...

Abstract	Background and purpose: Mild cognitive impairment (MCI) is a condition with diverse clinical outcomes and subgroups. Here we investigated the topographic distribution of tau in vivo using the positron emission tomography (PET) tracer [¹⁸F]THK5351 in MCI subgroups. Methods: This study included 96 participants comprising 38 with amnestic MCI (aMCI), 21 with nonamnestic MCI (naMCI), and 37 with normal cognition (NC) who underwent 3.0-T MRI, [¹⁸F]THK5351 PET, and detailed neuropsychological tests. [¹⁸F]flutemetamol PET was also performed in 62 participants. The aMCI patients were further divided into three groups: 1) verbal-aMCI, only verbal memory impairment; 2) visual-aMCI, only visual memory impairment; and 3) both-aMCI, both visual and verbal memory impairment. Voxel-wise statistical analysis and region-of-interest -based analyses were performed to evaluate the retention of [¹⁸F]THK5351 in the MCI subgroups. Subgroup analysis of amyloid-positive and -negative MCI patients was also performed. Correlations between [¹⁸F]THK5351 retention and different neuropsychological tests were evaluated using statistical parametric mapping analyses. Results: [¹⁸F]THK5351 retention in the lateral temporal, mesial temporal, parietal, frontal, posterior cingulate cortices and precuneus was significantly greater in aMCI patients than in NC subjects, whereas it did not differ significantly between naMCI and NC participants. [¹⁸F] THK5351 retention was greater in the both-aMCI group than in the verbal-aMCI and visualaMCI groups, and greater in amyloid-positive than amyloid-negative MCI patients. The cognitive function scores were significantly correlated with cortical [¹⁸F]THK5351 retention. Conclusions: [¹⁸F]THK5351 PET might be useful for identifying distinct topographic patterns of [¹⁸F]THK5351 retention in subgroups of MCI patients who are at greater risk of the progression to Alzheimer's dementia.
Language	English
Publishing date	2020-04-21
Publishing country	Korea (South)
Document type	Journal Article
ZDB-ID	2500489-X
ISSN	2005-5013 ; 1738-6586
ISSN (online)	2005-5013
ISSN	1738-6586
DOI	10.3988/jcn.2020.16.2.202
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Article: F-18 FDG PET/CT in NK/T-Cell Lymphoma that Progressed from Epstein-Barr Virus-Associated Hemophagocytic Lymphohistiocytosis.

Kim, Il-Hyun / An, Young-Sil / Lee, Su Jin / Yoon, Joon-Kee

Nuclear medicine and molecular imaging

2021 Volume 56, Issue 1, Page(s) 59–62

Abstract: ... and diagnosis are crucial for management. Although the role of F-18 fluorodeoxyglucose (FDG ... on disease status and possible triggers. Herein, we report an F-18 FDG PET/CT study on a case of NK/T-cell ...

Abstract	Hemophagocytic lymphohistiocytosis (HLH) is a syndrome involving an uncontrolled immune response with variable triggers. HLH is rare but highly fatal, even with proper treatment; therefore, early recognition and diagnosis are crucial for management. Although the role of F-18 fluorodeoxyglucose (FDG) positron emission tomography/computed tomography (PET/CT) in HLH is poorly defined, it can provide valuable information on disease status and possible triggers. Herein, we report an F-18 FDG PET/CT study on a case of NK/T-cell lymphoma that progressed from Epstein-Barr virus-associated HLH.
Language	English
Publishing date	2021-11-17
Publishing country	Germany
Document type	Case Reports
ZDB-ID	2541855-5
ISSN	1869-3482 ; 1869-3474
ISSN (online)	1869-3482
ISSN	1869-3474
DOI	10.1007/s13139-021-00725-3
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Article: ¹⁸F-Trifluoromethanesulfinate Enables Direct C–H ¹⁸F-Trifluoromethylation of Native Aromatic Residues in Peptides

Journal of the American Chemical Society. 2020 Jan. 08, v. 142, no. 3

2020

Abstract: ¹⁸F labeling strategies for unmodified peptides with [¹⁸F]fluoride require ¹⁸F-labeled prosthetics ... to target aromatic residues applying C–H ¹⁸F-trifluoromethylation. We report a one-step route to [¹⁸F ... CF₃SO₂NH₄ from [¹⁸F]fluoride and its application to direct [¹⁸F]CF₃ incorporation at tryptophan or tyrosine ...

Abstract	¹⁸F labeling strategies for unmodified peptides with [¹⁸F]fluoride require ¹⁸F-labeled prosthetics for bioconjugation more often with cysteine thiols or lysine amines. Here we explore selective radical chemistry to target aromatic residues applying C–H ¹⁸F-trifluoromethylation. We report a one-step route to [¹⁸F]CF₃SO₂NH₄ from [¹⁸F]fluoride and its application to direct [¹⁸F]CF₃ incorporation at tryptophan or tyrosine residues using unmodified peptides as complex as recombinant human insulin. The fully automated radiosynthesis of octreotide[Trp(2-CF₂¹⁸F)] enables in vivo positron emission tomography imaging.
Keywords	amines ; automation ; carbon-hydrogen bond activation ; chemical bonding ; cysteine ; fluorides ; humans ; image analysis ; insulin ; isotope labeling ; lysine ; octreotide ; positron-emission tomography ; thiols ; tryptophan ; tyrosine
Language	English
Dates of publication	2020-0108
Size	p. 1180-1185.
Publishing place	American Chemical Society
Document type	Article
ZDB-ID	3155-0
ISSN	1520-5126 ; 0002-7863
ISSN (online)	1520-5126
ISSN	0002-7863
DOI	10.1021/jacs.9b11709
Database	NAL-Catalogue (AGRICOLA)

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Article ; Online: Determination of the Ratio of b-Quark Fragmentation Fractions f(s)/f(d) in pp Collisions at √s=7 TeV with the ATLAS Detector.

Aad, G / Abbott, B / Abdallah, J / Abdinov, O / Aben, R / Abolins, M / AbouZeid, O S / Abramowicz, H / Abreu, H / Abreu, R / Abulaiti, Y / Acharya, B S / Adamczyk, L / Adams, D L / Adelman, J / Adomeit, S / Adye, T / Affolder, A A / Agatonovic-Jovin, T /

Agricola, J / Aguilar-Saavedra, J A / Ahlen, S P / Ahmadov, F / Aielli, G / Akerstedt, H / Åkesson, T P A / Akimov, A V / Alberghi, G L / Albert, J / Albrand, S / Alconada Verzini, M J / Aleksa, M / Aleksandrov, I N / Alexa, C / Alexander, G / Alexopoulos, T / Alhroob, M / Alimonti, G / Alio, L / Alison, J / Alkire, S P / Allbrooke, B M M / Allport, P P / Aloisio, A / Alonso, A / Alonso, F / Alpigiani, C / Altheimer, A / Alvarez Gonzalez, B / Álvarez Piqueras, D / Alviggi, M G / Amadio, B T / Amako, K / Amaral Coutinho, Y / Amelung, C / Amidei, D / Amor Dos Santos, S P / Amorim, A / Amoroso, S / Amram, N / Amundsen, G / Anastopoulos, C / Ancu, L S / Andari, N / Andeen, T / Anders, C F / Anders, G / Anders, J K / Anderson, K J / Andreazza, A / Andrei, V / Angelidakis, S / Angelozzi, I / Anger, P / Angerami, A / Anghinolfi, F / Anisenkov, A V / Anjos, N / Annovi, A / Antonelli, M / Antonov, A / Antos, J / Anulli, F / Aoki, M / Aperio Bella, L / Arabidze, G / Arai, Y / Araque, J P / Arce, A T H / Arduh, F A / Arguin, J-F / Argyropoulos, S / Arik, M / Armbruster, A J / Arnaez, O / Arnal, V / Arnold, H / Arratia, M / Arslan, O / Artamonov, A / Artoni, G / Asai, S / Asbah, N / Ashkenazi, A / Åsman, B / Asquith, L / Assamagan, K / Astalos, R / Atkinson, M / Atlay, N B / Augsten, K / Aurousseau, M / Avolio, G / Axen, B / Ayoub, M K / Azuelos, G / Baak, M A / Baas, A E / Baca, M J / Bacci, C / Bachacou, H / Bachas, K / Backes, M / Backhaus, M / Bagiacchi, P / Bagnaia, P / Bai, Y / Bain, T / Baines, J T / Baker, O K / Baldin, E M / Balek, P / Balestri, T / Balli, F / Banas, E / Banerjee, Sw / Bannoura, A A E / Bansil, H S / Barak, L / Barberio, E L / Barberis, D / Barbero, M / Barillari, T / Barisonzi, M / Barklow, T / Barlow, N / Barnes, S L / Barnett, B M / Barnett, R M / Barnovska, Z / Baroncelli, A / Barone, G / Barr, A J / Barreiro, F / Barreiro Guimarães da Costa, J / Bartoldus, R / Barton, A E / Bartos, P / Basalaev, A / Bassalat, A / Basye, A / Bates, R L / Batista, S J / Batley, J R / Battaglia, M / Bauce, M / Bauer, F / Bawa, H S / Beacham, J B / Beattie, M D / Beau, T / Beauchemin, P H / Beccherle, R / Bechtle, P / Beck, H P / Becker, K / Becker, M / Becker, S / Beckingham, M / Becot, C / Beddall, A J / Beddall, A / Bednyakov, V A / Bee, C P / Beemster, L J / Beermann, T A / Begel, M / Behr, J K / Belanger-Champagne, C / Bell, W H / Bella, G / Bellagamba, L / Bellerive, A / Bellomo, M / Belotskiy, K / Beltramello, O / Benary, O / Benchekroun, D / Bender, M / Bendtz, K / Benekos, N / Benhammou, Y / Benhar Noccioli, E / Benitez Garcia, J A / Benjamin, D P / Bensinger, J R / Bentvelsen, S / Beresford, L / Beretta, M / Berge, D / Bergeaas Kuutmann, E / Berger, N / Berghaus, F / Beringer, J / Bernard, C / Bernard, N R / Bernius, C / Bernlochner, F U / Berry, T / Berta, P / Bertella, C / Bertoli, G / Bertolucci, F / Bertsche, C / Bertsche, D / Besana, M I / Besjes, G J / Bessidskaia Bylund, O / Bessner, M / Besson, N / Betancourt, C / Bethke, S / Bevan, A J / Bhimji, W / Bianchi, R M / Bianchini, L / Bianco, M / Biebel, O / Biedermann, D / Bieniek, S P / Biglietti, M / Bilbao De Mendizabal, J / Bilokon, H / Bindi, M / Binet, S / Bingul, A / Bini, C / Biondi, S / Black, C W / Black, J E / Black, K M / Blackburn, D / Blair, R E / Blanchard, J-B / Blanco, J E / Blazek, T / Bloch, I / Blocker, C / Blum, W / Blumenschein, U / Bobbink, G J / Bobrovnikov, V S / Bocchetta, S S / Bocci, A / Bock, C / Boehler, M / Bogaerts, J A / Bogavac, D / Bogdanchikov, A G / Bohm, C / Boisvert, V / Bold, T / Boldea, V / Boldyrev, A S / Bomben, M / Bona, M / Boonekamp, M / Borisov, A / Borissov, G / Borroni, S / Bortfeldt, J / Bortolotto, V / Bos, K / Boscherini, D / Bosman, M / Boudreau, J / Bouffard, J / Bouhova-Thacker, E V / Boumediene, D / Bourdarios, C / Bousson, N / Boveia, A / Boyd, J / Boyko, I R / Bozic, I / Bracinik, J / Brandt, A / Brandt, G / Brandt, O / Bratzler, U / Brau, B / Brau, J E / Braun, H M / Brazzale, S F / Breaden Madden, W D / Brendlinger, K / Brennan, A J / Brenner, L / Brenner, R / Bressler, S / Bristow, K / Bristow, T M / Britton, D / Britzger, D / Brochu, F M / Brock, I / Brock, R / Bronner, J / Brooijmans, G / Brooks, T / Brooks, W K / Brosamer, J / Brost, E / Brown, J / Bruckman de Renstrom, P A / Bruncko, D / Bruneliere, R / Bruni, A / Bruni, G / Bruschi, M / Bruscino, N / Bryngemark, L / Buanes, T / Buat, Q / Buchholz, P / Buckley, A G / Buda, S I / Budagov, I A / Buehrer, F / Bugge, L / Bugge, M K / Bulekov, O / Bullock, D / Burckhart, H / Burdin, S / Burgard, C D / Burghgrave, B / Burke, S / Burmeister, I / Busato, E / Büscher, D / Büscher, V / Bussey, P / Butler, J M / Butt, A I / Buttar, C M / Butterworth, J M / Butti, P / Buttinger, W / Buzatu, A / Buzykaev, A R / Cabrera Urbán, S / Caforio, D / Cairo, V M / Cakir, O / Calace, N / Calafiura, P / Calandri, A / Calderini, G / Calfayan, P / Caloba, L P / Calvet, D / Calvet, S / Camacho Toro, R / Camarda, S / Camarri, P / Cameron, D / Caminal Armadans, R / Campana, S / Campanelli, M / Campoverde, A / Canale, V / Canepa, A / Cano Bret, M / Cantero, J / Cantrill, R / Cao, T / Capeans Garrido, M D M / Caprini, I / Caprini, M / Capua, M / Caputo, R / Cardarelli, R / Cardillo, F / Carli, T / Carlino, G / Carminati, L / Caron, S / Carquin, E / Carrillo-Montoya, G D / Carter, J R / Carvalho, J / Casadei, D / Casado, M P / Casolino, M / Castaneda-Miranda, E / Castelli, A / Castillo Gimenez, V / Castro, N F / Catastini, P / Catinaccio, A / Catmore, J R / Cattai, A / Caudron, J / Cavaliere, V / Cavalli, D / Cavalli-Sforza, M / Cavasinni, V / Ceradini, F / Cerio, B C / Cerny, K / Cerqueira, A S / Cerri, A / Cerrito, L / Cerutti, F / Cerv, M / Cervelli, A / Cetin, S A / Chafaq, A / Chakraborty, D / Chalupkova, I / Chang, P / Chapman, J D / Charlton, D G / Chau, C C / Chavez Barajas, C A / Cheatham, S / Chegwidden, A / Chekanov, S / Chekulaev, S V / Chelkov, G A / Chelstowska, M A / Chen, C / Chen, H / Chen, K / Chen, L / Chen, S / Chen, X / Chen, Y / Cheng, H C / Cheng, Y / Cheplakov, A / Cheremushkina, E / Cherkaoui El Moursli, R / Chernyatin, V / Cheu, E / Chevalier, L / Chiarella, V / Chiarelli, G / Chiodini, G / Chisholm, A S / Chislett, R T / Chitan, A / Chizhov, M V / Choi, K / Chouridou, S / Chow, B K B / Christodoulou, V / Chromek-Burckhart, D / Chudoba, J / Chuinard, A J / Chwastowski, J J / Chytka, L / Ciapetti, G / Ciftci, A K / Cinca, D / Cindro, V / Cioara, I A / Ciocio, A / Cirotto, F / Citron, Z H / Ciubancan, M / Clark, A / Clark, B L / Clark, P J / Clarke, R N / Cleland, W / Clement, C / Coadou, Y / Cobal, M / Coccaro, A / Cochran, J / Coffey, L / Cogan, J G / Colasurdo, L / Cole, B / Cole, S / Colijn, A P / Collot, J / Colombo, T / Compostella, G / Conde Muiño, P / Coniavitis, E / Connell, S H / Connelly, I A / Consorti, V / Constantinescu, S / Conta, C / Conti, G / Conventi, F / Cooke, M / Cooper, B D / Cooper-Sarkar, A M / Cornelissen, T / Corradi, M / Corriveau, F / Corso-Radu, A / Cortes-Gonzalez, A / Cortiana, G / Costa, G / Costa, M J / Costanzo, D / Côté, D / Cottin, G / Cowan, G / Cox, B E / Cranmer, K / Cree, G / Crépé-Renaudin, S / Crescioli, F / Cribbs, W A / Crispin Ortuzar, M / Cristinziani, M / Croft, V / Crosetti, G / Cuhadar Donszelmann, T / Cummings, J / Curatolo, M / Cuthbert, C / Czirr, H / Czodrowski, P / D'Auria, S / D'Onofrio, M / Da Cunha Sargedas De Sousa, M J / Da Via, C / Dabrowski, W / Dafinca, A / Dai, T / Dale, O / Dallaire, F / Dallapiccola, C / Dam, M / Dandoy, J R / Dang, N P / Daniells, A C / Danninger, M / Dano Hoffmann, M / Dao, V / Darbo, G / Darmora, S / Dassoulas, J / Dattagupta, A / Davey, W / David, C / Davidek, T / Davies, E / Davies, M / Davison, P / Davygora, Y / Dawe, E / Dawson, I / Daya-Ishmukhametova, R K / De, K / de Asmundis, R / De Benedetti, A / De Castro, S / De Cecco, S / De Groot, N / de Jong, P / De la Torre, H / De Lorenzi, F / De Pedis, D / De Salvo, A / De Sanctis, U / De Santo, A / De Vivie De Regie, J B / 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/ Shamim, M / Shan, L Y / Shang, R / Shank, J T / Shapiro, M / Shatalov, P B / Shaw, K / Shaw, S M / Shcherbakova, A / Shehu, C Y / Sherwood, P / Shi, L / Shimizu, S / Shimmin, C O / Shimojima, M / Shiyakova, M / Shmeleva, A / Shoaleh Saadi, D / Shochet, M J / Shojaii, S / Shrestha, S / Shulga, E / Shupe, M A / Shushkevich, S / Sicho, P / Sidebo, P E / Sidiropoulou, O / Sidorov, D / Sidoti, A / Siegert, F / Sijacki, Dj / Silva, J / Silver, Y / Silverstein, S B / Simak, V / Simard, O / Simic, Lj / Simion, S / Simioni, E / Simmons, B / Simon, D / Sinervo, P / Sinev, N B / Sioli, M / Siragusa, G / Sisakyan, A N / Sivoklokov, S Yu / Sjölin, J / Sjursen, T B / Skinner, M B / Skottowe, H P / Skubic, P / Slater, M / Slavicek, T / Slawinska, M / Sliwa, K / Smakhtin, V / Smart, B H / Smestad, L / Smirnov, S Yu / Smirnov, Y / Smirnova, L N / Smirnova, O / Smith, M N K / Smith, R W / Smizanska, M / Smolek, K / Snesarev, A A / Snidero, G / Snyder, S / Sobie, R / Socher, F / Soffer, A / Soh, D A / Sokhrannyi, G / Solans, C A / Solar, M / Solc, J / Soldatov, E Yu / Soldevila, U / Solodkov, A A / Soloshenko, A / Solovyanov, O V / Solovyev, V / Sommer, P / Song, H Y / Soni, N / Sood, A / Sopczak, A / Sopko, B / Sopko, V / Sorin, V / Sosa, D / Sosebee, M / Sotiropoulou, C L / Soualah, R / Soukharev, A M / South, D / Sowden, B C / Spagnolo, S / Spalla, M / Spangenberg, M / Spanò, F / Spearman, W R / Sperlich, D / Spettel, F / Spighi, R / Spigo, G / Spiller, L A / Spousta, M / Spreitzer, T / St Denis, R D / Staerz, S / Stahlman, J / Stamen, R / Stamm, S / Stanecka, E / Stanescu, C / Stanescu-Bellu, M / Stanitzki, M M / Stapnes, S / Starchenko, E A / Stark, J / Staroba, P / Starovoitov, P / Staszewski, R / Stavina, P / Steinberg, P / Stelzer, B / Stelzer, H J / Stelzer-Chilton, O / Stenzel, H / Stewart, G A / Stillings, J A / Stockton, M C / Stoebe, M / Stoicea, G / Stolte, P / Stonjek, S / Stradling, A R / Straessner, A / Stramaglia, M E / Strandberg, J / Strandberg, S / Strandlie, A 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I / Tsulaia, V / Tsuno, S / Tsybychev, D / Tudorache, A / Tudorache, V / Tuna, A N / Tupputi, S A / Turchikhin, S / Turecek, D / Turra, R / Turvey, A J / Tuts, P M / Tykhonov, A / Tylmad, M / Tyndel, M / Ueda, I / Ueno, R / Ughetto, M / Ugland, M / Ukegawa, F / Unal, G / Undrus, A / Unel, G / Ungaro, F C / Unno, Y / Unverdorben, C / Urban, J / Urquijo, P / Urrejola, P / Usai, G / Usanova, A / Vacavant, L / Vacek, V / Vachon, B / Valderanis, C / Valencic, N / Valentinetti, S / Valero, A / Valery, L / Valkar, S / Valladolid Gallego, E / Vallecorsa, S / Valls Ferrer, J A / Van Den Wollenberg, W / Van Der Deijl, P C / van der Geer, R / van der Graaf, H / van Eldik, N / van Gemmeren, P / Van Nieuwkoop, J / van Vulpen, I / van Woerden, M C / Vanadia, M / Vandelli, W / Vanguri, R / Vaniachine, A / Vannucci, F / Vardanyan, G / Vari, R / Varnes, E W / Varol, T / Varouchas, D / Vartapetian, A / Varvell, K E / Vazeille, F / Vazquez Schroeder, T / Veatch, J / Veloce, L M / Veloso, F / Velz, T / 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Watson, I J / Watson, M F / Watts, G / Watts, S / Waugh, B M / Webb, S / Weber, M S / Weber, S W / Webster, J S / Weidberg, A R / Weinert, B / Weingarten, J / Weiser, C / Weits, H / Wells, P S / Wenaus, T / Wengler, T / Wenig, S / Wermes, N / Werner, M / Werner, P / Wessels, M / Wetter, J / Whalen, K / Wharton, A M / White, A / White, M J / White, R / White, S / Whiteson, D / Wickens, F J / Wiedenmann, W / Wielers, M / Wienemann, P / Wiglesworth, C / Wiik-Fuchs, L A M / Wildauer, A / Wilkens, H G / Williams, H H / Williams, S / Willis, C / Willocq, S / Wilson, A / Wilson, J A / Wingerter-Seez, I / Winklmeier, F / Winter, B T / Wittgen, M / Wittkowski, J / Wollstadt, S J / Wolter, M W / Wolters, H / Wosiek, B K / Wotschack, J / Woudstra, M J / Wozniak, K W / Wu, M / Wu, S L / Wu, X / Wu, Y / Wyatt, T R / Wynne, B M / Xella, S / Xu, D / Xu, L / Yabsley, B / Yacoob, S / Yakabe, R / Yamada, M / Yamaguchi, D / Yamaguchi, Y / Yamamoto, A / Yamamoto, S / Yamanaka, T / Yamauchi, K / Yamazaki, 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Physical review letters

2015 Volume 115, Issue 26, Page(s) 262001

Abstract: ... used to determine the ratio of fragmentation fractions f(s)/f(d). From the observed B(s)(0)→J/ψϕ and B ... d)(0)→J/ψK(*0) yields, the quantity (f(s)/f(d))[B(B(s)(0)→J/ψϕ)/B(B(d)(0)→J/ψK(*0))] is measured ... ψK(*0))] yields (f(s)/f(d))=0.240±0.004(stat)±0.010(syst)±0.017(th). This result is based on a new ...

Abstract	With an integrated luminosity of 2.47 fb(-1) recorded by the ATLAS experiment at the LHC, the exclusive decays B(s)(0)→J/ψϕ and B(d)(0)→J/ψK(0) of B mesons produced in pp collisions at √s=7 TeV are used to determine the ratio of fragmentation fractions f(s)/f(d). From the observed B(s)(0)→J/ψϕ and B(d)(0)→J/ψK(0) yields, the quantity (f(s)/f(d))[B(B(s)(0)→J/ψϕ)/B(B(d)(0)→J/ψK(0))] is measured to be 0.199±0.004(stat)±0.008(syst). Using a recent theory prediction for [B(B(s)(0)→J/ψϕ)/B(B(d)(0)→J/ψK(0))] yields (f(s)/f(d))=0.240±0.004(stat)±0.010(syst)±0.017(th). This result is based on a new approach that provides a significant improvement of the world average.
Language	English
Publishing date	2015-12-31
Publishing country	United States
Document type	Journal Article
ZDB-ID	208853-8
ISSN	1079-7114 ; 0031-9007
ISSN (online)	1079-7114
ISSN	0031-9007
DOI	10.1103/PhysRevLett.115.262001
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Article ; Online: Intratympanic administration of alpha-lipoic acid-loaded pluronic F-127 nanoparticles ameliorates acute hearing loss.

Jung, So Young / Yoo, Jihye / Yang, Keum-Jin / Jang, Seok-Young / Yi, Gawon / Kim, Dong-Kee / Koo, Heebeom

Nanomedicine : nanotechnology, biology, and medicine

2020 Volume 32, Page(s) 102329

Abstract: We used antioxidant-containing nanoparticles (NPs) to treat acute hearing loss. Alpha-lipoic acid (ALA) served as the antioxidant; we employed Pluronic F127 to fabricate NPs. In vitro, ALA-NPs protected cells of the organ of Corti in HEI-OC1 mice, ... ...

Abstract	We used antioxidant-containing nanoparticles (NPs) to treat acute hearing loss. Alpha-lipoic acid (ALA) served as the antioxidant; we employed Pluronic F127 to fabricate NPs. In vitro, ALA-NPs protected cells of the organ of Corti in HEI-OC1 mice, triggering nuclear translocation of NRF2 and increases in the levels of antioxidant proteins, including Nrf2, HO-1, SOD-1, and SOD-2. In vivo, the hearing of mice that received ALA-NP injections into the middle ear cavity was better preserved after induction of ototoxicity than in control animals. The cochlear Nrf2 level increased in test mice, indicating that the ALA-NPs protected hearing via the antioxidant mechanism observed in vitro. ALA-NPs effectively protected against acute hearing loss by activating the Nrf2/HO-1 pathway.
MeSH term(s)	Animals ; Antioxidants/pharmacology ; Cell Death/drug effects ; Cell Line ; Cell Nucleus/drug effects ; Cell Nucleus/metabolism ; Disease Models, Animal ; Hearing Loss/drug therapy ; Hearing Loss/pathology ; Male ; Mice, Inbred C57BL ; NF-E2-Related Factor 2/metabolism ; Nanoparticles/chemistry ; Nanoparticles/ultrastructure ; Poloxamer/chemistry ; Thioctic Acid/administration & dosage ; Thioctic Acid/pharmacology ; Thioctic Acid/therapeutic use ; Tympanic Membrane/pathology ; Mice
Chemical Substances	Antioxidants ; NF-E2-Related Factor 2 ; Poloxamer (106392-12-5) ; Thioctic Acid (73Y7P0K73Y)
Language	English
Publishing date	2020-11-10
Publishing country	United States
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID	2183417-9
ISSN	1549-9642 ; 1549-9634
ISSN (online)	1549-9642
ISSN	1549-9634
DOI	10.1016/j.nano.2020.102329
Database	MEDical Literature Analysis and Retrieval System OnLINE

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Article ; Online: Clinical usefulness of F-18 FDG PET in lymphoepithelioma-like gastric carcinoma.

Park, Soyeon / Lee, Dakeun / Lee, Kee Myung / Han, Sang-Uk / Lee, Jei Hee / Lee, Su Jin / An, Young-Sil / Yoon, Joon-Kee

European journal of radiology

2017 Volume 94, Page(s) 160–166

Abstract: ... the clinical usefulness of F-18 FDG positron emission tomography/computed tomography (PET/CT) in LELC ... of stomach.: Materials and methods: A total of 28 patients (mean age=59years) who underwent preoperative F ... 18 FDG PET/CT were enrolled retrospectively. Nine patients underwent follow-up F-18 FDG PET/CT ...

Abstract	Purpose: Lymphoepithelioma-like carcinoma (LELC) is a rare type of gastric cancer. We evaluated the clinical usefulness of F-18 FDG positron emission tomography/computed tomography (PET/CT) in LELC of stomach. Materials and methods: A total of 28 patients (mean age=59years) who underwent preoperative F-18 FDG PET/CT were enrolled retrospectively. Nine patients underwent follow-up F-18 FDG PET/CT. Pathologic information was obtained through gastrectomy and the association with Epstein-Barr virus (EBV) was investigated in 26 patients. Results: PET/CT detected 85.0% (17/20) of advanced gastric cancers (AGC) and 12.5% (1/8) of early gastric cancers (EGC). Most tumors (23/26, 88.5%) were EBV-associated. The maximum standardized uptake value of FDG-avid tumors was 7.5±3.0. The sensitivity and specificity of PET/CT for the presence of lymph node metastasis was 47.8% (11/23) and 100.0% (13/13), respectively. PET/CT also detected a hepatic sarcomatoid carcinoma in one patient. The specificity of PET/CT for distant metastasis or second malignancy was 96.3%. Follow-up PET/CT detected malignant lesions in 3 of 9 patients; a liver metastasis, recurrent hepatic sarcomatoid carcinomas and a metachronous cholangiocarcinoma. PET/CT correctly excluded recurrence in the rest of the patients (6/6). The sensitivity and specificity of PET/CT for detecting recurrence or second malignancy was 100% and 100%, respectively. Conclusion: F-18 FDG PET/CT would be a useful tool in evaluating distant metastasis or recurrence in patients with gastric LELC.
Language	English
Publishing date	2017-09
Publishing country	Ireland
Document type	Journal Article
ZDB-ID	138815-0
ISSN	1872-7727 ; 0720-048X
ISSN (online)	1872-7727
ISSN	0720-048X
DOI	10.1016/j.ejrad.2017.06.022
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Article: Relationship Between Changes in Myocardial F-18 Fluorodeoxyglucose Uptake and Radiation Dose After Adjuvant Three-Dimensional Conformal Radiotherapy in Patients with Breast Cancer.

Jo, In Young / Lee, Jeong Won / Kim, Woo Chul / Min, Chul Kee / Kim, Eun Seog / Yeo, Seung-Gu / Lee, Sang Mi

Journal of clinical medicine

2020 Volume 9, Issue 3

Abstract: ... myocardial F-18 fluorodeoxyglucose (FDG) uptake after radiotherapy (RT) in breast cancer patients. The data ...

Abstract	This study aimed to assess the relationship between radiation dose and changes in the irradiated myocardial F-18 fluorodeoxyglucose (FDG) uptake after radiotherapy (RT) in breast cancer patients. The data of 55 patients with left and 48 patients with right breast cancer who underwent curative surgical resection and adjuvant three-dimensional conformal RT and staging (PET1), post-adjuvant chemotherapy (PET2), post-RT (PET3), and surveillance (PET4) FDG positron emission tomography/computed tomography (PET/CT) were retrospectively reviewed. The median interval between PET1 and curative surgical resection, between the end of adjuvant chemotherapy and PET2, between the end of RT and PET3, and between the end of RT and PET4 were five days, 13 days, 132 days, and 353 days, respectively. The myocardial-to-blood pool uptake ratio was measured in all patients. For patients with left breast cancer, the 30 Gy- (30 Gy) and 47.5 Gy-irradiated myocardium-to-low-irradiated myocardium (47.5 Gy) FDG uptake ratios were additionally measured. There were no differences in the myocardial-to-blood pool uptake ratios between left and right breast cancer on all PET scans. For left breast cancer, higher 30 Gy and 47.5 Gy uptake ratios were observed on PET3 than on PET1 and PET2. Both uptake ratios decreased on PET4 compared to PET3, but, were still higher compared to PET1. On PET3 and PET4, the 47.5 Gy were higher than the 30 Gy uptake ratios, while there were no differences between them on PET1 and PET2. Although the whole myocardium FDG uptake showed no significant change, the irradiated myocardium FDG uptake significantly increased after RT and was related to radiation dose to the myocardium in breast cancer patients. These results might be an imaging evidence that supports the increased risk of heart disease after RT in patients with left breast cancer.
Language	English
Publishing date	2020-03-02
Publishing country	Switzerland
Document type	Journal Article
ZDB-ID	2662592-1
ISSN	2077-0383
ISSN	2077-0383
DOI	10.3390/jcm9030666
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Article: Recent Survey of Effective Doses of F-18 FDG Torso PET/CT in Korea and the Current Recommendations for CT Protocols of PET/CT.

Chong, Ari / Park, Jung Mi / Pak, Kyoungjune / Kim, Yong-Il / Kwon, Hyun Woo / Lee, Eun Seong / Nam, Ki Pyo / Lee, Ho-Young / Lee, Hong Jae / Yoo, Ik Dong / Eo, Jae Seon / Kim, Ji Young / Yoon, Joon-Kee / Kim, Kyeong Min / Kim, Seong Min / Kim, Tae-Sung

Nuclear medicine and molecular imaging

2020 Volume 54, Issue 5, Page(s) 224–232

Abstract: Purpose: This study aimed to construct a database of the effective doses (ED) from F-18 ...

Abstract	Purpose: This study aimed to construct a database of the effective doses (ED) from F-18 fluorodeoxyglucose (FDG) torso positron emission tomography/computed tomography (PET/CT) in Korea to provide data that supports the reduction of the CT dose of PET/CT and optimization of PET/CT protocols in Korea. Methods: We investigated data of ED and CT parameters of FDG PET/CT. The data were analyzed by body weight groups. Results: A total of 31 hospitals participated in the survey (99 adults). The mean total EDs (± SD) were 8.77 ± 2.76, 10.93 ± 3.14, and 12.57 ± 3.79 mSv for the 55-, 70-, and 85-kg groups, respectively. The FDG EDs were 4.80 ± 0.98, 6.05 ± 1.15, and 6.89 ± 1.52 mSv, and the CT EDs were 4.00 ± 2.12, 4.88 ± 2.51, and 5.68 ± 2.89 mSv, respectively. Of the enrolled hospitals, 54.5% used ultra-low-dose CT protocols, and their CT ED was significantly lower than low-dose CT group in all groups (2.9 ± 1.0, 3.2 ± 1.1, and 3.3 ± 1.0 mSv vs. 6.6 ± 1.6, 7.2 ± 2.1, and 7.9 ± 2.2 mSv, all Conclusions: These results and current recommendations can be helpful for optimizing PET/CT diagnostic reference level (DRL) and reducing unnecessary PET/CT radiation exposure.
Language	English
Publishing date	2020-07-20
Publishing country	Germany
Document type	Journal Article
ZDB-ID	2541855-5
ISSN	1869-3482 ; 1869-3474
ISSN (online)	1869-3482
ISSN	1869-3474
DOI	10.1007/s13139-020-00654-7
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