{"database":"Pride","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Xlsx":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD068152/20250319_Mikes_1744_parasite.xlsx","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD068152/20250317_Mikes_1744-peptides2.xlsx"],"Txt":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD068152/checksum.txt"],"Raw":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD068152/1744-McES4.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD068152/1744-McH1.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD068152/1744-McES2.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD068152/1744-McH2.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD068152/1744-McES1.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD068152/1744-McES3.raw"],"Other":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD068152/20250318_Mikes_1744_jen_tasemnice.sps","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD068152/20250320_Mikes_tasemnice.sne","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD068152/20250317_1744-Mikes_databaze_Parasite.sne","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD068152/20250318_Mikes_1744-peptides2.sps","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD068152/20250318_Mikes_1744_parasite.sps"]},"type":"primary"},"statusCodeValue":200,"statusCode":"OK"}],"scores":null,"additional":{"labhead_mail":["vojte.vajs@gmail.com"],"submitter":["Jana Jasprova"],"technology_type":["Mass Spectrometry","Bottom-up proteomics","Data-independent acquisition"],"software":[""],"submitter_keywords":["Tapeworm","Tumor suppression","Kunitz","Transcriptome","Tetrathyridium","Proteome","Metastasis","Mesocestoides","Cancer"],"full_dataset_link":["https://www.ebi.ac.uk/pride/archive/projects/PXD068152"],"tissue":["Cestode"],"sample_protocol":["Collection of parasite material for proteomic analyses To obtain excretory-secretory products of tetrathyridia (McES), the larvae were harvested from intraperitoneally infected ICR mice 3 months post infection, washed 5x with sterile PBS, placed in 75 cm3 culture flasks (Eppendorf® Cell Culture Flask T-75) in DMEM  supplemented with 100 U/ml of penicillin-streptomycin and cultured at 37 °C, 5% CO2. The following day, they were transferred into new flasks in order to remove left-over adhered immune cells. The medium was collected and replaced every other day for two weeks, passed through a 0.22 μm sterile syringe-mounted filter (Sigma-Aldrich) and stored at -80 °C. The samples were concentrated with Amicon Ultra (Merck-Millipore, MWCO 10 kDa) and the medium replaced with sterile PBS. Protease inhibitors were added (cOmplete ULTRA Tablets, Mini, EDTA-free, EASYpack Protease Inhibitor Cocktail, Sigma-Aldrich). Each of four McES biological replicates was based on secretions of 900 tetrathyridia. For the preparation of M. corti homogenate, the larvae were washed in sterile PBS, placed into a solution of protease inhibitors in sterile PBS and sonicated at 60 W, 3 x 30 s. After centrifugation at 16 000 x g for 20 min the supernatant was collected and sterile filtered. Two biological replicates of the soluble homogenate fraction (McH) were used for MS analysis. Nanoflow liquid chromatography-tandem mass spectrometry of ESPs and soluble homogenate fractions from M. corti tetrathyridia Protein digestion The samples were lysed by boiling at 95°C for 10 min in 100mM triethylammonium bicarbonate (TEAB) containing 2% sodium deoxycholate (SDC), 40mM chloroacetamide, 10mM Tris(2-carboxyethyl)phosphine (TCEP) and further sonicated (Bandelin Sonoplus Mini 20, MS 1.5). Protein concentration was determined using BCA protein assay kit (Thermo) and 10 µg of protein per sample was used for MS sample preparation. The sample volume was adjusted to 65 µl by adding 100mM TEAB containing 2% SDC. Samples were further processed using SP3 beads on the Thermo KingFisher Flex automated Extraction & Purification System in a 96 well plate. Briefly, 65 µl of sample was added to 65 µl of 100 % ethanol and mixed with the SP3 beads. After binding, the beads were washed three times with 80% ethanol. After washing, samples were digested in 50mM TEAB at 40 °C with 1 µg of trypsin for 2 h, then another 1 µg of trypsin was added and left overnight. Samples after digestion were acidified with trifluoroacetic acid (TFA) to 1% final concentration and peptides were desalted using in-house made stage tips packed with C18 disks (Empore) (Rappsilber et al. 2007).  nLC/MS-MS Nano Reversed phase columns (Ion Opticks, Aurora Ultimate TS 25×75 C18 UHPLC column) were used for LC/MS-MS analysis. Mobile phase buffer A was composed of water and 0.1% formic acid. Mobile phase B was composed of acetonitrile and  0.1% formic acid. Samples were loaded onto the trap column (C18 PepMap100, 5 μm particle size, 300 μm x 5 mm, Thermo Scientific) for 4 min at 18 μl/min. The loading buffer was composed of water, 2% acetonitrile and 0.1% TFA. Peptides were eluted with Mobile phase B gradient from 4% to 35% B in 60 min. Eluting peptide cations were converted to gas-phase ions by electrospray ionization and analyzed on a Thermo Orbitrap Ascend (Thermo Scientific) by data independent approach. Survey scans of peptide precursors from 350 to 1400 m/z were performed in Orbitrap at 60K resolution (at 200 m/z) with a 4 × 105  ion count target. DIA scans were performed in Orbitrap at 30K resolution. AGC target was set to 1000 % and maximum injection time mode to Auto. Precursor mass range 400 – 1000 m/z was covered by 30 windows 20 Da wide. Activation type was set to HCD with 28 % collision energy."],"repository":["Pride"],"quantification_method":["Not available"],"modification":[""],"data_protocol":["All data were analyzed and quantified with the Spectronaut 19 software (Bruderer et al. 2015) using directDIA analysis. Data was searched against the M. corti database (PRJEB510, downloaded from WormBase in March 2025, containing 22 215 entries). Enzyme specificity was set as C-terminal to Arg and Lys, also allowing cleavage at proline bonds and a maximum of two missed cleavages. Carbamidomethylation of cysteines was set as fixed modification and N- terminal protein acetylation and methionine oxidation as variable modifications. FDR was set to 1 % for PSM, peptide and protein. Quantification was performed on MS2 level. Precursor PEP cutoff and precursor and protein cutoff were set to 0.01. Protein PEP was set to 0.05. Data were exported and data analysis was performed using Perseus 1.6.15.0 (Tyanova et al. 2016)."],"omics_type":["Proteomics"],"labhead":["Vojtěch Vajs"],"instrument_platform":[""],"labhead_affiliation":["Department of Parasitology, Faculty of Science, Charles University, Viničná 7, 12844 Prague 2, Czech Republic"],"submission_type":["PARTIAL"],"species":["Mesocestoides Corti","Mus Musculus (mouse)"],"submitter_mail":["vanikova@natur.cuni.cz"],"publication":["42036657 Vajs V, Mikeš L, Leontovyč R, Tulpová M, Korená L, Tolde O, Macháček T, Brábek J, Rösel D, Horák P. Integrated transcriptomic and proteomic analysis of cancer-suppressive Mesocestoides corti larvae. Parasit Vectors. 2026 19(1):244 10.1186/s13071-026-07391-4"],"submitter_affiliation":["Charles University, Faculty of Science"],"submitter_country":["Czechia"],"pubmed_abstract":["<h4>Background</h4>The larvae of Mesocestoides corti have been previously shown to abrogate the growth and metastasis of the highly aggressive B16F10 melanoma in mice. In order to investigate the potential ways in which this effect is mediated, we present, to the best of our knowledge, the most comprehensive analyses of M. corti larval molecular data so far, while listing and exploring various potentially immunomodulatory molecules found therein. We show expression and protein abundance in larvae under in vivo and in vitro conditions. A promising ortholog, M. corti Kunitz-type chymotrypsin-specific inhibitor 1 (McKI-C1) of a known cancer-suppressive Kunitz protein from Echinococcus granulosus is also tested, both in vitro and in vivo.<h4>Methods</h4>In order to explore the potential effector mechanisms and molecules behind its cancer-suppressive capabilities, we analyzed the M. corti larval transcriptome in the C57BL/6J and ICR mouse strains, as well as in vitro. The proteomic profiles of whole homogenate and excretory-secretory products of tetrathyridia were analyzed by nano-shotgun liquid chromatography with tandem mass spectrometry and thoroughly annotated. A Kunitz protein candidate (McKI-C1) was recombinantly expressed in Escherichia coli, biochemically characterized, and functionally tested for its anti-cancer effect with mouse melanoma B16F10 cells and mouse ovarian carcinoma ID8 cells.<h4>Results</h4>We present, to the best of our knowledge, the most extensive list of experimentally verified M. corti protein products. Many proteins potentially responsible for this tapeworm's immune-related cancer-suppressive abilities and immunomodulation were found within its proteome and transcriptome. These include numerous members of the superfamily of cysteine-rich secretory proteins, such as glioma pathogenesis-related-like proteins, and Kunitz-domain proteins. Functional tests of recombinant McKI-C1 performed both in vitro and in vivo did not confirm its expected tumor-suppressing properties. Therefore, the exact effectors of this tapeworm's likely immune-mediated anti-tumor capabilities need to be examined in further studies.<h4>Conclusions</h4>The transcriptomic and proteomic analysis of M. corti larvae carried out in the present study produced an extensive list of promising immunomodulatory or cancer-suppressive molecules. While the molecule chosen for analysis in the present study, McKI-C1, did not show any effect in vitro or in vivo, the immunomodulatory or cancer-suppressive potential of the other experimentally verified molecules remains of interest."],"pubmed_title":["Integrated transcriptomic and proteomic analysis of cancer-suppressive Mesocestoides corti larvae."],"pubmed_authors":["Vajs Vojtěch V, Mikeš Libor L, Leontovyč Roman R, Tulpová Madina M, Korená Lucie L, Tolde Ondřej O, Macháček Tomáš T, Brábek Jan J, Rösel Daniel D, Horák Petr P"],"additional_accession":[]},"is_claimable":false,"name":"The cancer-suppressive tapeworm Mesocestoides corti: larval transcriptome, proteome, and functional characterization of its McKI-C1 Kunitz-type protease inhibitor","description":"Cancer remains positioned as the leading cause of death worldwide, with nearly 10 million deaths and an estimated 20 million new cases yearly. Here, we present analyses of molecular data from the tumor-suppressing larvae of the tapeworm Mesocestoides corti, the intraperitoneal infection of which has previously demonstrated the ability to abrogate the growth and metastasis of the highly aggressive B16F10 melanoma in mice. In order to explore the potential effector mechanisms and molecules behind its cancer-suppressive capabilities, we analyzed the M. corti larval transcriptome in the C57BL/6J and ICR mouse strains, as well as in vitro, and the proteomic profiles of whole worm homogenate and its excretory-secretory products. We present, thus far, the most extensive list of experimentally verified M. corti protein products. These were searched for molecules potentially responsible for the tapeworm’s immune-related cancer-suppressive abilities. Many proteins with potential immunomodulatory properties were found within its proteome, including those from the cysteine-rich secretory CAP family, such as GLIPR-like proteins. Furthermore, functional tests of McKI-C1, an ortholog of the anti-cancer Kunitz inhibitor EgKI-1 from Echinococcus granulosus, were performed both in vitro and in vivo, to ascertain whether it could express a similar effect. While McKI-C1 did not show itself as an effector molecule in the tapeworm’s cancer-suppressive abilities, the extensive list of potentially functional molecules prompts further exploration.","dates":{"publication":"2026-06-15","submission":"2025-09-08"},"accession":"PXD068152","cross_references":{"TAXONOMY":["NEWT:108018","NEWT:377960","NEWT:1131","NEWT:190486","NEWT:2737160","NEWT:2042546","NEWT:148942","NEWT:295546","NEWT:258594","NEWT:1126","NEWT:1129","NEWT:89187","NEWT:309807","NEWT:89184","NEWT:309800","NEWT:1323429","NEWT:876138","NEWT:44271","NEWT:193516","NEWT:2315688","NEWT:44270","NEWT:592321","NEWT:1073882","NEWT:6819","NEWT:93217","NEWT:428386","NEWT:1117","NEWT:498257","NEWT:10036","NEWT:32264","NEWT:10034","NEWT:661410","NEWT:488003","NEWT:224326","NEWT:376619","NEWT:3765","NEWT:2433","NEWT:3767","NEWT:433727","NEWT:135622","NEWT:672127","NEWT:656061","NEWT:37965","NEWT:656064","NEWT:3760","NEWT:36630","NEWT:381198","NEWT:418106","NEWT:10029","NEWT:913645","NEWT:2492962","NEWT:641809","NEWT:44250","NEWT:317447","NEWT:698761","NEWT:5530","NEWT:868565","NEWT:135674","NEWT:1562698","NEWT:1177","NEWT:11308","NEWT:12637","NEWT:2164133","NEWT:1180","NEWT:2767846","NEWT:1343074","NEWT:314344","NEWT:108061","NEWT:224308","NEWT:3134131","NEWT:49928","NEWT:160621","NEWT:110368","NEWT:1916073","NEWT:1310161","NEWT:1230383","NEWT:77133","NEWT:1310165","NEWT:114727","NEWT:5516","NEWT:498211","NEWT:347256","NEWT:5518","NEWT:398007","NEWT:1527468","NEWT:498217","NEWT:498216","NEWT:11320","NEWT:1410384","NEWT:1310173","NEWT:161934","NEWT:156587","NEWT:1148","NEWT:5508","NEWT:135666","NEWT:419481","NEWT:5507","NEWT:1140","NCBITaxon:2157","NEWT:2066563","NEWT:1143","NEWT:1462472","NEWT:1336795","NEWT:644042","NEWT:709964","NEWT:3712","NEWT:3711","NEWT:3714","NEWT:65121","NEWT:3716","NEWT:3715","NEWT:2065263","NEWT:1549675","NEWT:177437","NEWT:9014","NEWT:10891","NEWT:118221","NEWT:34869","NEWT:226126","NEWT:1616117","NEWT:34865","NEWT:28174","NEWT:550537","NEWT:284812","NEWT:284811","NEWT:3701","NEWT:3702","NEWT:1245466","NEWT:3704","NEWT:1246791","NEWT:34875","NEWT:1431297","NEWT:9005","NEWT:34871","NEWT:9006","NEWT:33548","NEWT:1883426","NEWT:657321","NEWT:1423687","NEWT:657322","NEWT:10886","NEWT:3708","NEWT:536231","NEWT:219813","NEWT:1301262","NEWT:319224","NEWT:2305479","NEWT:215451","NEWT:460519","NEWT:272843","NEWT:272844","NEWT:1348799","NEWT:55784","NEWT:485","NEWT:2499525","NEWT:467144","NEWT:142786","NEWT:28196","NEWT:2853422","NEWT:487","NEWT:1679718","NEWT:387344","NEWT:657318","NEWT:480","NEWT:67767","NEWT:46835","NEWT:216778","NEWT:376686","NEWT:237610","EFO:0001352","NEWT:219809","NEWT:219808","NEWT:119562","NEWT:1883446","NEWT:1233435","NEWT:118223","NEWT:141469","NEWT:272831","NEWT:987059","NEWT:491","NEWT:422203","NEWT:460523","NEWT:2423","NEWT:85694","NEWT:85692","NEWT:911045","NEWT:3750","NEWT:123606","NEWT:85698","NEWT:291146","NEWT:233271","NEWT:3745","NEWT:1715989","NCBITaxon:4751","NEWT:3747","NEWT:278161","NEWT:415978","NEWT:410289","NEWT:191701","NEWT:9054","NEWT:472","NEWT:29459","NEWT:34839","NEWT:476","NEWT:1380096","NEWT:28128","NEWT:470","NEWT:41122","NEWT:1328300","NEWT:748693","NCBITaxon:50557","NEWT:63363","NEWT:3735","NEWT:29491","NEWT:911022","NEWT:446","NEWT:153481","NEWT:714485","NEWT:445","NEWT:2003758","NEWT:29486","NEWT:63366","NEWT:64697","NEWT:63367","NEWT:29488","NEWT:215402","NEWT:3726","NEWT:30455","NEWT:28141","NEWT:9030","NEWT:9031","NEWT:3728","NEWT:108931","NEWT:219799","NEWT:1325292","NEWT:219798","NEWT:548","NEWT:150475","NEWT:546","NEWT:1431340","NEWT:256737","NEWT:51350","NEWT:8694","NEWT:8692","NEWT:542","NEWT:394503","NEWT:13076","NEWT:219785","NEWT:451515","NEWT:8673","NEWT:550","NEWT:10804","NEWT:554","NEWT:451516","NEWT:552","NEWT:1325291","NEWT:42410","NEWT:40686","NEWT:1225786","NEWT:771870","NEWT:8665","NEWT:51338","NEWT:377142","NEWT:9995","NEWT:28112","NEWT:49012","NEWT:28110","NEWT:10832","NEWT:311339","NEWT:507601","NEWT:520","NEWT:64657","NEWT:186441","NEWT:2585209","NEWT:643680","NEWT:214092","NEWT:40697","NEWT:13095","NEWT:162425","NEWT:242124","NEWT:9986","NEWT:8654","NEWT:536","NEWT:8658","NEWT:1268063","NEWT:8657","NEWT:9983","NEWT:8655","NEWT:80833","NEWT:479096","NEWT:28108","NEWT:28104","NEWT:1114957","NEWT:568703","NEWT:568708","NEWT:51315","NEWT:52641","NEWT:353152","NEWT:116597","NEWT:353153","NEWT:116598","NEWT:227377","NEWT:1774284","NEWT:27689","NEWT:207769","NEWT:40674","NEWT:51329","NCBITaxon:1763","NEWT:443906","NEWT:13037","NEWT:519","NEWT:941638","NEWT:511","NEWT:7394","NEWT:6063","NEWT:404330","NEWT:1328388","NEWT:13064","NEWT:529120","NEWT:300641","NEWT:39655","NEWT:38323","NEWT:206411","NEWT:80869","NEWT:214053","NEWT:80863","NEWT:665890","NEWT:52639","NEWT:52638","NEWT:8697","NEWT:861109","NEWT:8695","NEWT:1196866","NEWT:6039","NEWT:37003","NEWT:510516","NEWT:1045775","NEWT:1123869","NCBITaxon:1335626","NEWT:7370","NEWT:280406","NEWT:83906","NEWT:99488","NEWT:99487","NEWT:1134506","NEWT:255470","NEWT:762903","NEWT:27697","NEWT:86185","NEWT:9935","NEWT:266940","NEWT:287889","NEWT:9938","NEWT:1028307","NEWT:52603","NEWT:92867","NEWT:92866","NEWT:1344414","NEWT:202950","NEWT:741158","NEWT:1293091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