<?xml version="1.0" encoding="utf-8"?>
<doi_batch xmlns="http://www.crossref.org/schema/4.3.6" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:jats="http://www.ncbi.nlm.nih.gov/JATS1" xmlns:ai="http://www.crossref.org/AccessIndicators.xsd" xmlns:fr="http://www.crossref.org/fundref.xsd" version="4.3.6" xsi:schemaLocation="http://www.crossref.org/schema/4.3.6 https://www.crossref.org/schemas/crossref4.3.6.xsd">
  <head>
    <doi_batch_id>_1698904394</doi_batch_id>
    <timestamp>20231102055314000</timestamp>
    <depositor>
      <depositor_name>Rovedar</depositor_name>
      <email_address>Daryoushbabazadeh@gmail.com</email_address>
    </depositor>
    <registrant>Rovedar </registrant>
  </head>
  <body>
    <journal>
      <journal_metadata>
        <full_title>Journal of Lab Animal Research</full_title>
        <abbrev_title>J Lab Anim. Res</abbrev_title>
        <issn media_type="electronic">2980-9703</issn>
      </journal_metadata>
      <journal_issue>
        <publication_date media_type="online">
          <month>10</month>
          <day>25</day>
          <year>2023</year>
        </publication_date>
        <journal_volume>
          <volume>2</volume>
        </journal_volume>
        <issue>5</issue>
      </journal_issue>
      <journal_article xmlns:jats="http://www.ncbi.nlm.nih.gov/JATS1" xmlns:ai="http://www.crossref.org/AccessIndicators.xsd" publication_type="full_text" metadata_distribution_opts="any">
        <titles>
          <title>Anti-cancer Potential of Hydatid Cyst-Derived Antigens: In Vivo Insights</title>
        </titles>
        <contributors>
          <person_name contributor_role="author" sequence="first" language="en">
            <given_name>Zeinab</given_name>
            <surname>Hosseini</surname>
            <ORCID>https://orcid.org/0009-0003-6975-8960</ORCID>
          </person_name>
          <person_name contributor_role="author" sequence="additional" language="en">
            <given_name>Mohaddeseh</given_name>
            <surname>Jamali</surname>
            <ORCID>https://orcid.org/0009-0007-1453-7641</ORCID>
          </person_name>
          <person_name contributor_role="author" sequence="additional" language="en">
            <given_name>Nikoo</given_name>
            <surname>Sadat Hasheminezhad</surname>
            <ORCID>https://orcid.org/0009-0006-0139-2650</ORCID>
          </person_name>
          <person_name contributor_role="author" sequence="additional" language="en">
            <given_name>Razieh</given_name>
            <surname>Razmi</surname>
            <ORCID>https://orcid.org/0009-0001-8868-0746</ORCID>
          </person_name>
          <person_name contributor_role="author" sequence="additional" language="en">
            <given_name>Rezvan</given_name>
            <surname>Abbasi</surname>
            <ORCID>https://orcid.org/0009-0008-3434-2355</ORCID>
          </person_name>
          <person_name contributor_role="author" sequence="additional" language="en">
            <given_name>Negar</given_name>
            <surname>Jahani</surname>
            <ORCID>https://orcid.org/0000-0002-5076-3925</ORCID>
          </person_name>
          <person_name contributor_role="author" sequence="additional" language="en">
            <given_name>Mahsa</given_name>
            <surname>Mohammadian</surname>
          </person_name>
        </contributors>
        <jats:abstract xmlns:jats="http://www.ncbi.nlm.nih.gov/JATS1">
          <jats:p>The global healthcare challenge of cancer remains challenging, requiring innovative approaches to identify potential anticancer agents. The intriguing anti-tumor properties of hydatid cysts produced in their larval stage by Echinococcus granulosus (E. granulosus) have attracted the attention of many scientists in recent years. This review aimed to delve deeper into the in vivo anticancer effects of hydatid cyst-derived antigens and shed light on their mechanisms of action and therapeutic implications for various cancer types. Several bioactive molecules in E. granulosus antigens have shown significant anti-cancer activity in vivo. Several studies have shown that administering these antigens reduced tumor size while increasing overall survival in breast cancer models. The immune response against tumor cells in lung cancer murine models has also been enhanced by E. granulosus antigens, such as antigen B, leading to the regression of tumors and enhanced immunity. Colon cancer cells are sensitized to these antigens as indicated by in vivo studies, rendering standard chemotherapy more effective at inhibiting tumor growth. E. granulosus antigens also reduce tumor metastasis when applied to in vivo melanoma models. E. granulosus antigens have demonstrated in vivo efficacy as a potential anticancer agent, underscoring their potential as valuable therapeutic agents. There is still much to be discovered about the exact mechanisms of these antigens and their clinical applicability. However, the impressive results observed across a wide range of cancer types underscore the significance of further research into the antigens to overcome cancer in vivo. In conclusion, animal model studies reveal the promising potential of E. granulosus antigens, particularly hydatid cyst fluid, in inhibiting tumor growth in colon, breast, melanoma, and lung cancers through immune-mediated mechanisms and apoptosis induction. These findings open up new avenues for cancer therapy and immunotherapy research, emphasizing the role of parasite antigens in combatting various cancer types.</jats:p>
        </jats:abstract>
        <publication_date media_type="online">
          <month>10</month>
          <day>25</day>
          <year>2023</year>
        </publication_date>
        <pages>
          <first_page>33</first_page>
          <last_page>40</last_page>
        </pages>
        <fr:program name="fundref"/>
        <ai:program xmlns:ai="http://www.crossref.org/AccessIndicators.xsd" name="AccessIndicators">
          <ai:license_ref>https://creativecommons.org/licenses/by/4.0</ai:license_ref>
        </ai:program>
        <doi_data>
          <doi>10.58803/jlar.v2i5.26</doi>
          <resource>https://jlar.rovedar.com/index.php/JLAR/article/view/26</resource>
          <collection property="crawler-based">
            <item crawler="iParadigms">
              <resource>https://jlar.rovedar.com/index.php/JLAR/article/download/26/54</resource>
            </item>
          </collection>
          <collection property="text-mining">
            <item>
              <resource mime_type="application/pdf">https://jlar.rovedar.com/index.php/JLAR/article/download/26/54</resource>
            </item>
          </collection>
        </doi_data>
        <citation_list>
          <citation key="1370">
            <unstructured_citation>Bray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA and Jemal A. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA: Cancer J Clinic. 2018; 68(6): 394-424. DOI: https://doi.org/10.3322/caac.21492</unstructured_citation>
          </citation>
          <citation key="1371">
            <unstructured_citation>Ferlay J, Colombet M, Soerjomataram I, Mathers C, Parkin DM, Piñeros M, Znaor A and Bray F. Estimating the global cancer incidence and mortality in 2018: GLOBOCAN sources and methods. Int J Cancer. 2019; 144(8): 1941-1953. DOI: https://doi.org/10.1002/ijc.31937</unstructured_citation>
          </citation>
          <citation key="1372">
            <unstructured_citation>Hricak H, Ward ZJ, Atun R, Abdel-Wahab M, Muellner A and Scott AM. Increasing access to imaging for addressing the global cancer epidemic. Radiol Soci N Am. 2021; 301(3): 543-546. DOI: https://doi.org/10.1148/radiol.2021211351</unstructured_citation>
          </citation>
          <citation key="1373">
            <unstructured_citation>Sadr S and Borji H. Echinococcus granulosus as a Promising Therapeutic Agent against Triplenegative Breast Cancer. Curr Cancer Ther Rev. 2023; 19(4): 292-297. DOI: https://doi.org/10.2174/1573394719666230427094247</unstructured_citation>
          </citation>
          <citation key="1374">
            <unstructured_citation>Sadr S, Ghiassi S, Lotfalizadeh N, Simab PA, Hajjafari A and Borji H. Antitumor Mechanisms of Molecules Secreted by Trypanosoma cruzi in Colon and Breast Cancer: A Review. Anticancer Agents Med Chem. 2023; 23(15): 1710-1721. DOI: https://doi.org/10.2174/1871520623666230529141544</unstructured_citation>
          </citation>
          <citation key="1375">
            <unstructured_citation>Asouli A, Sadr S, Mohebalian H and Borji H. Anti-Tumor Effect of Protoscolex Hydatid Cyst Somatic Antigen on Inhibition Cell Growth of K562. Acta Parasitologica. 2023; 1-8. DOI: https://doi.org/10.1007/s11686-023-00680-3</unstructured_citation>
          </citation>
          <citation key="1376">
            <unstructured_citation>Sadr S, Yousefsani Z, Simab PA, Alizadeh HJR, Lotfalizadeh A and Borji H. Trichinella spiralis as a Potential Antitumor Agent: An Update. World’s Vet J. 2023; 13: 65-74. DOI: https://doi.org/10.54203/scil.2023.wvj7</unstructured_citation>
          </citation>
          <citation key="1377">
            <unstructured_citation>Yousofi Darani H, Soozangar N, Khorami S, Taji F, Yousofi M and Shirzad H. Hydatid cyst protoscolices induce cell death in WEHI-164 fibrosarcoma cells and inhibit the proliferation of baby hamster kidney fibroblasts in vitro. J Parasitol Res. 2012; 2012. DOI: https://doi.org/10.1155/2012/304183</unstructured_citation>
          </citation>
          <citation key="1378">
            <unstructured_citation>Ranasinghe SL and McManus DP. Echinococcus granulosus: cure</unstructured_citation>
          </citation>
          <citation key="1379">
            <unstructured_citation>for cancer revisited. Front Med. 2018; 5: 60. DOI: https://doi.org/10.3389/fmed.2018.00060</unstructured_citation>
          </citation>
          <citation key="1380">
            <unstructured_citation>Hosch W, Junghanss T, Stojkovic M, Brunetti E, Heye T, Kauffmann GW and Hull WE. Metabolic viability assessment of cystic echinococcosis using high‐field 1H MRS of cyst contents. NMR Biomed: Int J Devot Develop App Magnet Resonance In vivo. 2008; 21(7): 734-754. DOI: https://doi.org/10.1002/nbm.1252</unstructured_citation>
          </citation>
          <citation key="1381">
            <unstructured_citation>Shojaeian A, Barati N and Motavallihaghi S. Investigating the Inhibitory Effects of Hydatid Cyst Fluid and its Antigens on Cancer Progression: A Review. 2023; DOI: https://doi.org/10.20944/preprints202307.2141.v1</unstructured_citation>
          </citation>
          <citation key="1382">
            <unstructured_citation>Chookami MB, Sharafi SM, Sefiddashti RR, Jafari R, Bahadoran M, Pestechian N and Darani HY. Effect of two hydatid cyst antigens on the growth of melanoma cancer in C57/black mice. J Parasit Dis. 2016; 40: 1170-1173. DOI: https://doi.org/10.1007/s12639-015-0643-7</unstructured_citation>
          </citation>
          <citation key="1383">
            <unstructured_citation>Berriel E, Freire T, Chiale C, Rodríguez E, Morón G, Fernandez-Grana G, Crispo M, Berois N and Osinaga E. Human hydatid cyst fluid-induced therapeutic anti-cancer immune responses via NK1. 1+ cell activation in mice. Cancer Immunol, Immunothe 2021; 70(12): 3617-3627. DOI: https://doi.org/10.1007/s00262-021-02948-x</unstructured_citation>
          </citation>
          <citation key="1384">
            <unstructured_citation>Kudelka MR, Ju T, Heimburg-Molinaro J and Cummings RD. Simple sugars to complex disease—mucin-type O-glycans in cancer. Adv Cancer Res. 2015; 126: 153-135. DOI: https://doi.org/10.1016/bs.acr.2014.11.002</unstructured_citation>
          </citation>
          <citation key="1385">
            <unstructured_citation>Oliveira-Ferrer L, Legler K and Milde-Langosch K. Role of protein glycosylation in cancer metastasis. Semin Cancer Bio. 2017; 44: 141-152. DOI: https://doi.org/10.1016/j.semcancer.2017.03.002</unstructured_citation>
          </citation>
          <citation key="1386">
            <unstructured_citation>Casaravilla C, Freire T, Malgor R, Medeiros A, Osinaga E and Carmona C. Mucin-type O-glycosylation in helminth parasites from major taxonomic groups: evidence for widespread distribution of the Tn antigen (GalNAc-Ser/Thr) and identification of UDP-GalNAc: polypeptide N-acetylgalactosaminyltransferase activity. J Parasitol. 2003; 89(4): 709-714. DOI: https://doi.org/10.1645/GE-2970</unstructured_citation>
          </citation>
          <citation key="1387">
            <unstructured_citation>Parkinson J, Wasmuth J, Salinas G, Bizarro C and Sanford C. A Transcriptomic Analysis of Echinococcus granulosus Larval</unstructured_citation>
          </citation>
          <citation key="1388">
            <unstructured_citation>Stages. 2012; DOI: https://doi.org/10.1371/annotation/984cd209-4e98-467c-b462-c11090e43be7</unstructured_citation>
          </citation>
          <citation key="1389">
            <unstructured_citation>Hajizadeh M, Amni F, Sahlolbei M, Tavakoli-yaraki M, Mamaghani AJ, Sefiddashti RR and Rezaee H. Antigen Similarity In Hydatid Cyst Wall And Human Bone Tumours: A Short Report. 2021; DOI: https://doi.org/10.21203/rs.3.rs-411912/v1</unstructured_citation>
          </citation>
          <citation key="1390">
            <unstructured_citation>Noya V, Bay S, Festari MF, García EP, Rodriguez E, Chiale C, Ganneau C, Baleux F, Astrada S, Bollati-Fogolín M, Osinaga E and Freire T. Mucin-like peptides from Echinococcus granulosus induce anti-tumor activity. Int J Oncol. 2013; 43(3): 775-784. DOI: https://doi.org/10.3892/ijo.2013.2000</unstructured_citation>
          </citation>
          <citation key="1391">
            <unstructured_citation>Karadayi S, Arslan S, Sumer Z, Turan M, Sumer H and Karadayi K. Does hydatid disease have protective effects against lung cancer? Molecular biology reports. 2013; 40: 4701-4704. DOI: https://doi.org/10.1007/s11033-013-2565-8</unstructured_citation>
          </citation>
          <citation key="1392">
            <unstructured_citation>Zhang W and McManus DP. Recent advances in the immunology and diagnosis of echinococcosis. FEMS Immunol Med Microbiol. 2006; 47(1): 24-41. DOI: https://doi.org/10.1111/j.1574-695X.2006.00060.x</unstructured_citation>
          </citation>
          <citation key="1393">
            <unstructured_citation>Barati N, Tanzadehpanah H, Asl SS, Khazaei S and Motavallihaghi S. 2022;</unstructured_citation>
          </citation>
          <citation key="1394">
            <unstructured_citation>Wang Y, Xiao D, Shen Y, Han X, Zhao F, Li X, Wu W, Zhou H, Zhang J and Cao J. Proteomic analysis of the excretory/secretory products and antigenic proteins of Echinococcus granulosus adult worms from infected dogs. BMC Vet Res. 2015; 11: 1-7. DOI: https://doi.org/10.1186/s12917-015-0423-8</unstructured_citation>
          </citation>
          <citation key="1395">
            <unstructured_citation>Rahman WA, Elmajdoub L, Noor S and Wajidi M. Present status on the taxonomy and morphology of Echinococcus granulosus: A review. Austin J Vet Sci Anim Husb. 2015; 2(2). DOI:</unstructured_citation>
          </citation>
          <citation key="1396">
            <unstructured_citation>Tlamcani Z. Hydatidosis in Morocco: Review of literature and epidemiology. Afro-Egypt J Inf Endem Dis. 2016; 6(3): 152-155. DOI: https://doi.org/10.21608/aeji.2016.9962</unstructured_citation>
          </citation>
          <citation key="1397">
            <unstructured_citation>Grosso G, Gruttadauria S, Biondi A, Marventano S and Mistretta A. Worldwide epidemiology of liver hydatidosis including the Mediterranean area. World J Gastroenterol. 2012; 18(13): 1425-1437. DOI: https://doi.org/10.3748/wjg.v18.i13.1425</unstructured_citation>
          </citation>
          <citation key="1398">
            <unstructured_citation>Kumsa B and Mohammedzein A. Prevalence, organ distribution, risk factors, and financial losses of hydatid cysts in sheep and goats slaughtered in restaurants in Jimma, south western Oromia. Comparative Clin Pathol. 2012; 23(2): 333-339. DOI: https://doi.org/10.1007/s00580-012-1619-y</unstructured_citation>
          </citation>
          <citation key="1399">
            <unstructured_citation>Hughes J and Macdonald DW. A review of the interactions between free-roaming domestic dogs and wildlife. Bio Conser. 2013; 157: 341-351. DOI: https://doi.org/10.1016/j.biocon.2012.07.005</unstructured_citation>
          </citation>
          <citation key="1400">
            <unstructured_citation>Hayashi N, Kouguchi H, Imasato Y, Irie T, Yagi K, Nonaka N and Nakao R. Early-phase migration dynamics of Echinococcus multilocularis in two mouse strains showing different infection susceptibilities. Int J Parasitol. 2021; 51(11): 893-898. DOI: https://doi.org/10.1016/j.ijpara.2021.04.001</unstructured_citation>
          </citation>
          <citation key="1401">
            <unstructured_citation>Gessese AT, Mulate B, Nazir S and Asmare A. Major metacestodes in small ruminants slaughtered at Dessie municipal abattoir, Eastern Ethiopia: prevalence, cyst viability, organ distribution and economic implications. Compar Clin Pathol. 2015; 24: 659-668. DOI: https://doi.org/10.1007/s00580-014-1964-0</unstructured_citation>
          </citation>
          <citation key="1402">
            <unstructured_citation>Sadr S, Charbgoo A, Borji H and Hajjafari A. Interactions between innate immunity system and Echinococcus granulosus: permission for vaccine development. Series Med Sci. 2022; 3(1): 1-18. Avaialbale at: https://seriesscience.com/wp-content/uploads/2023/01/Interactions-between-Innate-Immunity.pdf</unstructured_citation>
          </citation>
          <citation key="1403">
            <unstructured_citation>Raether W and Hänel H. Epidemiology, clinical manifestations and diagnosis of zoonotic cestode infections: an update. Parasitol Res. 2003; 91(5): 412-438. DOI: https://doi.org/10.1007/s00436-003-0903-9</unstructured_citation>
          </citation>
          <citation key="1404">
            <unstructured_citation>Eckert J, Gemmell M, Meslin F-X, Pawlowski Z and Organization WH. WHO/OIE manual on echinococcosis in humans and animals: a public health problem of global concern. World Organis Anim Health. 2001; DOI:</unstructured_citation>
          </citation>
          <citation key="1405">
            <unstructured_citation>Siles-Lucas M, Casulli A, Conraths FJ and Muller N. Laboratory Diagnosis of Echinococcus spp. in Human Patients and Infected Animals. Adv Parasitol. 2017; 96: 159-257. DOI: https://doi.org/10.1016/bs.apar.2016.09.003</unstructured_citation>
          </citation>
          <citation key="1406">
            <unstructured_citation>Sweatman G and Williams R. Comparative studies on the biology and morphology of Echinococcus granulosus from domestic livestock, moose and reindeer. Parasitol. 1963; 53(3-4): 339-390. DOI: https://doi.org/10.1017/S0031182000073832</unstructured_citation>
          </citation>
          <citation key="1407">
            <unstructured_citation>Shojaeian A, Barati N and Motavallihaghi S. Investigating the Inhibitory Effects of Hydatid Cyst Fluid and its Antigens on Cancer Progression: A Review. 2023; DOI: https://doi.org/10.20944/preprints202307.2141.v1</unstructured_citation>
          </citation>
          <citation key="1408">
            <unstructured_citation>Siracusano A, Delunardo F, Teggi A, Ortona E. Host-parasite relationship in cystic echinococcosis: an evolving story. J Immunol Res. 2012; 639362. DOI: https://doi.org/10.1155/2012/639362</unstructured_citation>
          </citation>
          <citation key="1409">
            <unstructured_citation>Han X, Zhou Y and Liu W. Precision cardio-oncology: understanding the cardiotoxicity of cancer therapy. NPJ Precisi Oncol. 2017; 1(1): 31. DOI: https://doi.org/10.1038/s41698-017-0034-x</unstructured_citation>
          </citation>
          <citation key="1410">
            <unstructured_citation>Ikemoto S, Sugimura K, Yoshida N, Yasumoto R, Wada S, Yamamoto K and Kishimoto T. Anti-tumor effects of Scutellariae radix and its components baicalein, baicalin, and wogonin on bladder cancer cell lines. Urol. 2000; 55(6): 951-955. DOI: https://doi.org/10.1016/S0090-4295(00)00467-2</unstructured_citation>
          </citation>
          <citation key="1411">
            <unstructured_citation>Shooraj M, Hajipour E and Mahdavi SA. Immunological Examination of Echinococcus granulosus as a Candidate for Cancer Treatment and Vaccine Development: A Review Study. Tabari Biomed Stu Res J. 2022; 4(3): 40-48. DOI: https://doi.org/10.18502/tbsrj.v4i3.10516</unstructured_citation>
          </citation>
          <citation key="1412">
            <unstructured_citation>Guan W, Zhang X, Wang X, Lu S, Yin J and Zhang J. Employing parasite against cancer: a lesson from the canine tapeworm Echinococcus granulocus. Front Pharmacol. 2019; 10: 1137. DOI: https://doi.org/10.3389/fphar.2019.01137</unstructured_citation>
          </citation>
          <citation key="1413">
            <unstructured_citation>Darani HY and Yousefi M. Parasites and cancers: parasite antigens as possible targets for cancer immunotherapy. Future Oncol. 2012; 8(12): 1529-1535. DOI: https://doi.org/10.2217/fon.12.155</unstructured_citation>
          </citation>
          <citation key="1414">
            <unstructured_citation>Ditgen D, Anandarajah EM, Hansmann J, Winter D, Schramm G, Erttmann KD, Liebau E and Brattig NW. Multifunctional thioredoxin-like protein from the gastrointestinal parasitic nematodes Strongyloides ratti and Trichuris suis affects mucosal homeostasis. J Parasitol Res. 2016; 2016. DOI: https://doi.org/10.1155/2016/8421597</unstructured_citation>
          </citation>
          <citation key="1415">
            <unstructured_citation>Darani HY. Effect of hydatid cyst antigens on inhibition of melanoma cancer growth in mouse model. Cell Mol Biol. 2018; 64(12): 1-6. DOI: https://doi.org/10.14715/cmb/2018.64.12.1</unstructured_citation>
          </citation>
          <citation key="1416">
            <unstructured_citation>Van der Weijden J, Paulis LE, Verdoes M, van Hest JC and Figdor CG. The right touch: design of artificial antigen-presenting cells to stimulate the immune system. Chem Sci. 2014; 5(9): 3355-3367. DOI: https://doi.org/10.1039/C4SC01112K</unstructured_citation>
          </citation>
          <citation key="1417">
            <unstructured_citation>Farinon M, Oliveira P, Clarimundo V, Monteiro K, Zaha A, Ferreira H and Xavier RM. AB0135 Immunomodulatory and Antiinflammatory Properties of Antigen B, A Protein Secreted by Echinococcus Granulosus Larval Stage, in Experimental Arthritis. Annal Rheumatic Dis. 2014; 73(Suppl 2): 848-848. DOI: https://doi.org/10.1136/annrheumdis-2014-eular.3897</unstructured_citation>
          </citation>
          <citation key="1418">
            <unstructured_citation>Nono JK, Pletinckx K, Lutz MB and Brehm K. Excretory/secretory-products of Echinococcus multilocularis larvae induce apoptosis and tolerogenic properties in dendritic cells in vitro. PLoS Neglect Tropi Dis. 2012; 6(2): e1516. DOI: https://doi.org/10.1371/journal.pntd.0001516</unstructured_citation>
          </citation>
          <citation key="1419">
            <unstructured_citation>Wysocka J, Reilly PT and Herr W. Loss of HCF-1–chromatin association precedes temperature-induced growth arrest of tsBN67 cells. Mol Cell Bio. 2001; 21(11): 3820-3829. DOI: https://doi.org/10.1128/MCB.21.11.3820-3829.2001</unstructured_citation>
          </citation>
          <citation key="1420">
            <unstructured_citation>Huang S. Regulation of metastases by signal transducer and activator of transcription 3 signaling pathway: clinical implications. Clin Cancer Res. 2007; 13(5): 1362-1366. DOI: https://doi.org/10.1158/1078-0432.CCR-06-2313</unstructured_citation>
          </citation>
          <citation key="1421">
            <unstructured_citation>Gupta SC, Kim JH, Prasad S and Aggarwal BB. Regulation of survival, proliferation, invasion, angiogenesis, and metastasis of tumor cells through modulation of inflammatory pathways by nutraceuticals. Cancer Metastas Rev. 2010; 29: 405-434. DOI: https://doi.org/10.1007/s10555-010-9235-2</unstructured_citation>
          </citation>
          <citation key="1422">
            <unstructured_citation>Mouhid L, Gómez de Cedrón M, García-Carrascosa E, Reglero G, Fornari T and Ramírez de Molina A. Yarrow supercritical extract exerts antitumoral properties by targeting lipid metabolism in pancreatic cancer. PloS one. 2019; 14(3): e0214294. DOI: https://doi.org/10.1371/journal.pone.0214294</unstructured_citation>
          </citation>
          <citation key="1423">
            <unstructured_citation>Shakibapour M, Kefayat A, Reza Mofid M, Shojaie B, Mohamadi F, Maryam Sharafi S, Mahmoudzadeh M and Darani HY. Anti-cancer immunoprotective effects of immunization with hydatid cyst wall antigens in a non-immunogenic and metastatic triple-negative murine mammary carcinoma model. Int Immunopharmacol. 2021 ;99: 107955. DOI: https://doi.org/10.1016/j.intimp.2021.107955</unstructured_citation>
          </citation>
          <citation key="1424">
            <unstructured_citation>Gundogdu SB, Saylam B and Tez M. Cyst hydatid and cancer: The myth continues. Clin Chem Lab Med (CCLM). 2017; 55(7): e150-e1. DOI: https://doi.org/10.1515/cclm-2016-0626</unstructured_citation>
          </citation>
          <citation key="1425">
            <unstructured_citation>Diaz A, Casaravilla C, Barrios AA and Ferreira AM. Parasite molecules and host responses in cystic echinococcosis. Parasite Immunol. 2016; 38(3): 193-205. DOI: https://doi.org/10.1111/pim.12282</unstructured_citation>
          </citation>
          <citation key="1426">
            <unstructured_citation>Asghari A, Nourmohammadi H, Majidiani H, Shariatzadeh SA, Anvari D, Shamsinia S, Ghasemi E, Shams M and Basati G. Promising effects of parasite-derived compounds on tumor regression: a systematic review of in vitro and in vivo studies. Enviro Sci Pollut Res. 2022; 29(22): 32383-32396. DOI: https://doi.org/10.1007/s11356-021-17090-5</unstructured_citation>
          </citation>
          <citation key="1427">
            <unstructured_citation>Oikonomopoulou K, Yu H, Wang Z, Vasiliou SK, Brinc D, Christofi G, Theodorou M, Pavlou P, Hadjisavvas A, Demetriou CA, Kyriacou K and Diamandis EP. Association between Echinococcus granulosus infection and cancer risk–a pilot study in Cyprus. Clin Chem Lab Med (CCLM). 2016; 54(12): 1955-1961. DOI: https://doi.org/10.1515/cclm-2016-0125</unstructured_citation>
          </citation>
          <citation key="1428">
            <unstructured_citation>DeNardo DG and Coussens LM. Inflammation and breast cancer. Balancing immune response: crosstalk between adaptive and innate immune cells during breast cancer progression. Breast Cancer Res. 2007; 9: 1-10. DOI: https://doi.org/10.1186/bcr1746</unstructured_citation>
          </citation>
          <citation key="1429">
            <unstructured_citation>Rostami-Rad S, Jafari R and Darani HY. Th1/Th2-type cytokine profile in C57 black mice inoculated with live Echinococcus granulosus protoscolices. J Inf Pub Health. 2018; 11(6): 834-839. DOI: https://doi.org/10.1016/j.jiph.2018.06.007</unstructured_citation>
          </citation>
          <citation key="1430">
            <unstructured_citation>Koski GK, Koldovsky U, Xu S, Mick R and Sharma A, Fitzpatrick E, Weinstein S, Nisenbaum H, Levine BL, Fox K, Zhang P, Czerniecki BJ. A novel dendritic cell-based immunization approach for the induction of durable Th1-polarized anti-HER-2/neu responses in women with early breast cancer. J Immunothe (Hagerstown, Md: 1997). 2012; 35(1): 54. DOI: https://doi.org/10.1097/CJI.0b013e318235f512</unstructured_citation>
          </citation>
          <citation key="1431">
            <unstructured_citation>Berois N, Pittini A and Osinaga E. Targeting tumor glycans for cancer therapy: successes, limitations, and perspectives. Cancer. 2022; 14(3): 645. DOI: https://doi.org/10.3390/cancers14030645</unstructured_citation>
          </citation>
          <citation key="1432">
            <unstructured_citation>Nodeh FJ, Sharafi SM, Tuloee S, Hejazi SH, Dorosti Z and Darani HY. Effect of passive transfer of anti-hydatid cyst antigen antisera on melanoma tumor growth in animal model. World J Oncol Res. 2015; 2: 1-4. DOI:</unstructured_citation>
          </citation>
          <citation key="1433">
            <unstructured_citation>Yousefi M, Akbari M, Hadipour M, Dehkordi AB, Farahbakhsh Z and Darani HY. Parasites as potential targets for cancer immunotherapy. J Cancer Res Clin Oncol. 2023; 1-12. DOI: https://doi.org/10.1007/s00432-023-04694-2</unstructured_citation>
          </citation>
          <citation key="1434">
            <unstructured_citation>Dogan S, Cakir M, Kartal A, Oztas H and Oltulu P. Can Echinococcus Granulosus Infestation Prevent Pancreatic Cancer? An invivo Experimental Study. Asian Pac J Cancer Prev. 2023; 24(4): 1307-1312. DOI: https://doi.org/10.31557/APJCP.2023.24.4.1307</unstructured_citation>
          </citation>
          <citation key="1435">
            <unstructured_citation>Badri-Chookami M, Sharafi SM, Rafeie R, Bahadoran M, Pestechian N and Yousofi-Darani H. Effect of Alive Protoscoleces of Hydatid Cyst on the Growth of Melanoma Cells in Mouse Model. J Isfahan Med Sch.</unstructured_citation>
          </citation>
          <citation key="1436">
            <unstructured_citation>; 32(281): 486-492. Available at: https://jims.mui.ac.ir/ article_14312_8743986d61a8e1edda4d92b198eaed2e.pdf?lang=en</unstructured_citation>
          </citation>
          <citation key="1437">
            <unstructured_citation>Darani HY, Sharafi SM, Mokarian F, Yousefi M, Sharafi SA and Jafari R. Therapeutic effect of hydatid cyst liquid on melanoma tumor growth in mouse model. British J Med Res. 2016; 18(2): 1-7. DOI: https://doi.org/10.9734/BJMMR/2016/27220</unstructured_citation>
          </citation>
          <citation key="1438">
            <unstructured_citation>Daneshpour S, reza Mofid M, Andalib A, Eskandariyan A and Darani HY. Effect of hydatid cyst antigens on inhibition of melanoma cancer growth in mouse model. Cell Mol Bio. 2018; 64(12): 1-5. DOI: https://doi.org/10.14715/cmb/2018.64.12.1</unstructured_citation>
          </citation>
          <citation key="1439">
            <unstructured_citation>Berriel E, Russo S, Monin L, Festari MF, Berois N, Fernandez G, Freire T and Osinaga E. Anti-tumor activity of human hydatid cyst fluid in a murine model of colon cancer. Sci World J. 2013; 2013: 230176. DOI: https://doi.org/10.1155/2013/230176</unstructured_citation>
          </citation>
          <citation key="1440">
            <unstructured_citation>Rostamirad S, Daneshpour S, Mofid MR, Andalib A, Eskandariyan A, Mousavi S and Drani HY. Inhibition of mouse colon cancer growth following immunotherapy with a fraction of hydatid cyst fluid. Exp Parasitol. 2023; 249: 108501. DOI: https://doi.org/10.1016/j.exppara.2023.108501</unstructured_citation>
          </citation>
          <citation key="1441">
            <unstructured_citation>Berriel E, Freire T, Chiale C, Rodriguez E, Moron G, Fernandez-Grana G, Crispo M, Berois N and Osinaga E. Human hydatid cyst fluid-induced therapeutic anti-cancer immune responses via NK1.1(+) cell activation in mice. Cancer Immunol Immunother. 2021; 70(12): 3617-3627. DOI: https://doi.org/10.1007/s00262-021-02948-x</unstructured_citation>
          </citation>
          <citation key="1442">
            <unstructured_citation>Cao S, Gong W, Zhang X, Xu M, Wang Y, Xu Y, Cao J, Shen Y and Chen J. Arginase promotes immune evasion of Echinococcus granulosus in mice. Parasit Vector. 2020; 13(1): 49. DOI: https://doi.org/10.1186/s13071-020-3919-4</unstructured_citation>
          </citation>
          <citation key="1443">
            <unstructured_citation>Vafae Eslahi A, Ghaffarifar F, Muhammad Hassan Z and Dalimi A. Anticancer Activity of Hydatid Cyst Fluid along with Antigen B on Tumors Induced by 4T1 Breast Cancer Cell in a BALB/c Mice Model. Iran J Parasitol. 2022; 17(2): 240-249. DOI: https://doi.org/10.18502/ijpa.v17i2.9542</unstructured_citation>
          </citation>
          <citation key="1444">
            <unstructured_citation>Daneshpour S, Kefayat AH, Mofid MR, Rostami Rad S and Yousofi Darani H. Effect of Hydatid Cyst Fluid Antigens on Induction of Apoptosis on Breast Cancer Cells. Adv Biomed Res. 2019; 8: 27. DOI: https://doi.org/10.4103/abr.abr_220_18</unstructured_citation>
          </citation>
        </citation_list>
      </journal_article>
    </journal>
  </body>
</doi_batch>
