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AIMS Genetics

2018, Volume 5, Issue 1: 75-90. doi: 10.3934/genet.2018.1.75
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Esophageal cancer research today and tomorrow: Lessons from algae and other perspectives

  • 1.
    Centre for Genomic and Regenerative Medicine, School of Biomedicine, FEFU, 8 Sukhanova str, Vladivostok, Primorsky region, 690950, Russian Federation
  • 2.
    Laboratory of Pharmacology and Bioassays, School of Biomedicine, FEFU, 8 Sukhanova str, Vladivostok, Primorsky region, 690950, Russian Federation
  • 3.
    Microalgal Biotechnology Laboratory, The French Associates Institute for Agriculture and Biotechnology for Drylands, The J. Blaustein Institutes for Desert Research, Ben-Gurion University of the Negev, Sede-Boqer Campus, Midreshet Ben-Gurion 8499000, Israel
  • Received: 02 December 2017 Accepted: 01 March 2018 Published: 07 March 2018

  • Esophageal cancer is an increasing concern due to poor prognosis, aggressive disease modalities, and a lack of efficient therapeutics. The two types of esophageal cancer: esophageal squamous cell carcinoma (ESCC) and esophageal adenocarcinoma (EAC) are responsible for an estimated 450,000 annual deaths, with over 457,000 new patients diagnosed in 2015, making it the eighth most prevalent and the 10th most fatal cancer worldwide. As esophageal cancer prevalence continues to increase, and so does the pressing need for the development of new and effective strategies for the early diagnostics, prevention, and treatment of this cancer, as well for building the innovative research tools to understand the affected molecular mechanisms.
    This short review summarizes the current statistics and recent research of the problems and solutions related to the esophageal cancer, and offer a brief overview of its epidemiology, molecular alterations, and existing biomedical tools. We will discuss currently available research tools and discuss selected approaches we deem relevant to find new model systems and therapies for the future with the special focus on novel opportunities presented by the unique molecules found in algae, namely carbohydrates and lipids. Their remarkable chemical variability is connected to their striking structural and functional properties, which combined with the relative novelty of these compounds to cancer biology, warrants interest of the wide biomedical community to these molecules, especially in the esophageal cancer theory and practice.

    Citation: Vladlena Tiasto, Valeriia Mikhailova, Valeriia Gulaia, Valeriia Vikhareva, Boris Zorin, Alexandra Kalitnik, Alexander Kagansky. Esophageal cancer research today and tomorrow: Lessons from algae and other perspectives[J]. AIMS Genetics, 2018, 5(1): 75-90. doi: 10.3934/genet.2018.1.75

    Related Papers:

  • Esophageal cancer is an increasing concern due to poor prognosis, aggressive disease modalities, and a lack of efficient therapeutics. The two types of esophageal cancer: esophageal squamous cell carcinoma (ESCC) and esophageal adenocarcinoma (EAC) are responsible for an estimated 450,000 annual deaths, with over 457,000 new patients diagnosed in 2015, making it the eighth most prevalent and the 10th most fatal cancer worldwide. As esophageal cancer prevalence continues to increase, and so does the pressing need for the development of new and effective strategies for the early diagnostics, prevention, and treatment of this cancer, as well for building the innovative research tools to understand the affected molecular mechanisms.
    This short review summarizes the current statistics and recent research of the problems and solutions related to the esophageal cancer, and offer a brief overview of its epidemiology, molecular alterations, and existing biomedical tools. We will discuss currently available research tools and discuss selected approaches we deem relevant to find new model systems and therapies for the future with the special focus on novel opportunities presented by the unique molecules found in algae, namely carbohydrates and lipids. Their remarkable chemical variability is connected to their striking structural and functional properties, which combined with the relative novelty of these compounds to cancer biology, warrants interest of the wide biomedical community to these molecules, especially in the esophageal cancer theory and practice.


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    [1] Song Q, Jiang D, Wang H, et al. (2017) Chromosomal and genomic variations in esophageal squamous cell carcinoma: A review of technologies, applications, and prospections. J Cancer 8: 2492. doi: 10.7150/jca.19601
    [2] Hou X, Wen J, Ren Z, et al. (2017) Non-coding RNAs: New biomarkers and therapeutic targets for esophageal cancer. Oncotarget 8: 43571–43578.
    [3] Esophagus Cancer statictics in USA. Esophagus Cancer.org. [Online] June 14, 2017. Available from: www.cancer.org/cancer/esophaguscancer/detailedguide/esophagus-cancer-key-statistics.
    [4] Testa U, Castelli G, Pelosi E (2017) Esophageal cancer: Genomic and molecular characterization, stem cell compartment and clonal evolution. Medicinis 4.
    [5] Esophageal cancer statistics in UK. Cancer Research UK. [Online] Nov 22, 2017. Available from: www.cancerresearchuk.org/health-professional/cancer-statistics/statistics-by-cancer-type/oesophageal-cancer#heading-One.
    [6] Zhang Y (2013) Epidemiology of esophageal cancer. World J Gastroenterol 19: 5598–5606. doi: 10.3748/wjg.v19.i34.5598
    [7] Taylor PR, Abnet CC, Dawsey SM (2013) Squamous dysplasia â the precursor lesion for esophageal squamous cell carcinoma. Cancer Epidemiol Biomarkers Prev 22: 540–552. doi: 10.1158/1055-9965.EPI-12-1347
    [8] Siewert JR, Ott K (2007) Are squamous and adenocarcinomas of the esophagus the same disease? Semin Radiat Oncol 17: 38–44. doi: 10.1016/j.semradonc.2006.09.007
    [9] Zhao R, Young CB, Mee-Hyun L, et al. (2016) Implications of genetic and epigenetic alterations of CDKN2A (p16INK4a) in cancer. Ebiomedicine 8: 30–39. doi: 10.1016/j.ebiom.2016.04.017
    [10] Singhi AD, Foxwell TJ, Nason K, et al. (2015) Smad4 loss in esophageal adenocarcinoma is associated with an increased propensity for disease recurrence and poor survival. Am J Surg Pathol 39: 487–495. doi: 10.1097/PAS.0000000000000356
    [11] Streppel MM, Lata S, DelaBastide M, et al. (2014) Next-generation sequencing of endoscopic biopsies identifies ARID1A as a tumor-suppressor gene in Barrett's esophagus. Oncogene 33: 347–357. doi: 10.1038/onc.2012.586
    [12] Dulak AM, Stojanov P, Peng S, et al. (2013) Exome and whole-genome sequencing of esophageal adenocarcinoma identifies recurrent driver events and mutational complexity. Nat Genet 45: 478–486. doi: 10.1038/ng.2591
    [13] Gao YB, Chen ZL, Li JG, et al. (2014) Genetic landscape of esophageal squamous cell carcinoma. Nat Genet 46: 1097–1102. doi: 10.1038/ng.3076
    [14] Sasaki Y, Tamura M, Koyama R, et al. (2016) Genomic characterization of esophageal squamous cell carcinoma: Insights from next-generation sequencing. World J Gastroenterol 22: 2284–2293. doi: 10.3748/wjg.v22.i7.2284
    [15] Nazila N, Katrien VR, Mohammad V, et al. (2013) Expression, Tissue Distribution and Function of miR-21 in Esophageal Squamous Cell Carcinoma. PLoS One 8: e73009. doi: 10.1371/journal.pone.0073009
    [16] Rubenstein JH, Shaheen NJ (2015) Epidemiology, diagnosis, and management of esophageal adenocarcinoma. Gastroenterology 149: 302–317. doi: 10.1053/j.gastro.2015.04.053
    [17] Watanabe M (2015) Risk factors and molecular mechanisms of esophageal cancer: Differences between the histologic subtypes. J Cancer Metastasis Treat 1: 1–7.
    [18] Halland M, Katzka D, Iyer PG (2015) Recent developments in pathogenesis, diagnosis and therapy of Barrett's esophagus. World J Gastroenterol 21: 6479–6490. doi: 10.3748/wjg.v21.i21.6479
    [19] Palethorpe HM, Drew PA, Smith E (2017) Androgen Signaling in Esophageal Adenocarcinoma Cell Lines In Vitro. Dig Dis Sci 62: 3402–3414. doi: 10.1007/s10620-017-4794-5
    [20] Wang RH (2015) From reflux esophagitis to Barrett's esophagus and esophageal adenocarcinoma. World J Gastroenterol 21: 5210–5219. doi: 10.3748/wjg.v21.i17.5210
    [21] Pietsch EC, Humbey O, Murphy ME (2006) Polymorphisms in the p53 pathway. Oncogene 25: 1602–1611. doi: 10.1038/sj.onc.1209367
    [22] Bond G, Hu W, Bond EE, et al. (2004) A single nucleotide polymorphism in the MDM2 promoter. Cell 119: 591–602. doi: 10.1016/j.cell.2004.11.022
    [23] Akbari M, Malekzadeh R, Lepage P, et al. (2011) Mutations in Fanconi anemia genes and the risk of esophageal cancer. Hum Genet 129: 573–582. doi: 10.1007/s00439-011-0951-7
    [24] Dandara C, Li DP, Walther G, et al. (2006) Gene-environment interaction: The role of SULT1A1 and CYP3A5 polymorphisms as risk modifiers for squamous cell. Carcinogenesis 27: 791–797. doi: 10.1093/carcin/bgi257
    [25] O'Neill JR, Pak HS, Pairocastineira E, et al. (2017) Quantitative Shotgun Proteomics Unveils Candidate Novel Esophageal Adenocarcinoma (EAC)-Specific Proteins. Mol Cell Proteomics Mcp 16: 1138–1150. doi: 10.1074/mcp.M116.065078
    [26] Ke X, Yan R, Sun Z, et al. (2017) Esophageal Adenocarcinoma-Derived Extracellular Vesicle MicroRNAs Induce a Neoplastic Phenotype in Gastric Organoids. Neoplasia 19: 941–949. doi: 10.1016/j.neo.2017.06.007
    [27] Lee Y, Urbanska AM, Hayakawa Y, et al. (2016) Gastrin stimulates a cholecystokinin-2-receptor-expressing cardia progenitor cell and promotes progression of Barrett's-like esophagus. Oncotarget 8: 203–214.
    [28] D'Journo XB, Thomas PA (2014) Current management of esophageal cancer. J Thorac Dis 6: S253–S264.
    [29] Sohda M, Kuwano H (2016) Current Status and Future Prospects for Esophageal Cancer Treatment. Ann Thorac Cardiovasc Surg 23: 1–11. doi: 10.1093/icvts/ivw098
    [30] Akutsu Y, Matsubara H (2015) Chemoradiotherapy and surgery for T4 esophageal cancer in Japan. Surg Today 45: 1360–1365. doi: 10.1007/s00595-015-1116-4
    [31] Sithranga BN, Kathiresan K (2011) Anticancer drugs from marine flora: An overview. J Oncol 2010: 214186.
    [32] Tebbutt NC, Price TJ, Ferraro DA, et al. (2016) Panitumumab added to docetaxel, cisplatin and fluoropyrimidine in oesophagogastric cancer: ATTAX3 phase II trial. Br J Cancer 114: 505–509. doi: 10.1038/bjc.2015.440
    [33] Niu J, Gelbspan D, Weitz D, et al. (2014) HER2-positive, trastuzumab-resistant metastatic esophageal cancer presenting with brain metastasis after durable response to dual HER2 blockade: A case report. J Gastrointest Oncol 5: E103–E110.
    [34] Idelevich E, Kashtan H, Klein Y, et al. (2012) Prospective phase II study of neoadjuvant therapy with cisplatin, 5-FU, and bevacizumab for locally advanced resectable esophageal cancer. Onkologie 35: 427–431. doi: 10.1159/000340072
    [35] Davidson M, Starling N (2016) Trastuzumab in the management of gastroesophageal cancer: Patient selection and perspectives. OncoTargets Ther 9: 7235–7245. doi: 10.2147/OTT.S100643
    [36] Ilson DH, Kelsen D, Shah M, et al. (2011) A phase 2 trial of erlotinib in patients with previously treated squamous cell and adenocarcinoma of the esophagusr. Cancer 117: 1409–1414. doi: 10.1002/cncr.25602
    [37] Rodriguez CP, Adelstein DJ, Rice TW, et al. (2010) A phase II study of perioperative concurrent chemotherapy, gefitinib, and hyperfractionated radiation followed by maintenance gefitinib in locoregionally advanced esophagus and gastroesophageal junction cancer. J Thorac Oncol 5: 229–235. doi: 10.1097/JTO.0b013e3181c5e334
    [38] Altiok S, Mezzadra H, Jagannath S, et al. (2010) A novel pharmacodynamic approach to assess and predict tumor response to the epidermal growth factor receptor inhibitor gefitinib in patients with esophageal cancer. Int J Oncol 36: 19.
    [39] Martinucci I, Bortoli ND, Russo S, et al. (2016) Barrett's esophagus in 2016: From pathophysiology to treatment. World J Gastrointest Pharmacol Ther 7: 190–206. doi: 10.4292/wjgpt.v7.i2.190
    [40] Kwiatek MA, Roman S, Fareeduddin A, et al. (2011) An alginate-antacid formulation (Gaviscon Double Action Liquid) can eliminate the postprandial "acid pocket" in symptomatic GERD patients. Aliment Pharmacol Ther 34: 59–66. doi: 10.1111/j.1365-2036.2011.04678.x
    [41] Yuan H, Song J, Li X, et al. (2006) Immunomodulation and antitumor activity of k-carrageenan oligosaccharides. Cancer Lett 243: 228–234. doi: 10.1016/j.canlet.2005.11.032
    [42] Monnerat C, Faivre S, Temam S, et al. (2002) End points for new agents in induction chemotherapy for locally advanced head and neck cancers. Ann Oncol 13: 995–1006. doi: 10.1093/annonc/mdf172
    [43] Neergheen-Bhujun V, Awan AT, Baran Y, et al. (2017) Biodiversity, drug discovery, and the future of global health: Introducing the biodiversity to biomedicine consortium, a call to action. J Global Health 7: 020304. doi: 10.7189/jogh.07.020304
    [44] Jimeno J, Faircloth G, Sousa-Faro JF, et al. (2004) New Marine Derived Anticancer Therapeutics-A Journey from the Sea to Clinical Trials. Mar Drugs 2: 14–29. doi: 10.3390/md201014
    [45] Kijjoa A, Sawangwong P (2004) Drugs and Cosmetics from the Sea. Mar Drugs 2: 328–336.
    [46] Kuo YH, Liang TW, Liu KC, et al. (2011) Isolation and identification of a novel antioxidant with antitumour activity from Serratia ureilytica using squid pen as fermentation substrate. Mar Biotechnol 13: 451–461. doi: 10.1007/s10126-010-9316-9
    [47] Kwon HJ, Bae SY, Kim KH, et al. (2007) Induction of apoptosis in HeLa cells by ethanolic extract of Corallina pilulifera. Food Chem 104: 196–201. doi: 10.1016/j.foodchem.2006.11.031
    [48] Lins KOAL, Bezerra DP, Alves APNN, et al. (2009) Antitumor properties of a sulfated polysaccharide from the red seaweed Champia feldmannii (Diaz-Pifferer). J Appl Toxicol Jat 29: 20–26. doi: 10.1002/jat.1374
    [49] Thoppil RJ, Bishayee A (2011) Terpenoids as potential chemopreventive and therapeutic agents in liver cancer. World J Hepatol 3: 228–249. doi: 10.4254/wjh.v3.i9.228
    [50] Zandi K, Ahmadzadeh S, Tajbakhsh S, et al. (2010) Anticancer activity of Sargassum oligocystum water extract against human cancer cell lines. Eur Rev Med Pharmacol Sci 14: 669–673.
    [51] Usoltseva RV, Anastyuk SD, Shevchenko NM, et al. (2017) Polysaccharides from brown algae Sargassum duplicatum: The structure and anticancer activity in vitro. Carbohydr Polym 175: 547–556. doi: 10.1016/j.carbpol.2017.08.044
    [52] Alves C, Pinteus S, Horta A, et al. (2016) High cytotoxicity and anti-proliferative activity of algae extracts on an in vitro model of human hepatocellular carcinoma. Springerplus 5: 1339. doi: 10.1186/s40064-016-2938-2
    [53] Gamal-Eldeen AM, Ahmed EF, Abo-Zeid MA (2009) In vitro cancer chemopreventive properties of polysaccharide extract from the brown alga, Sargassum latifolium. Food Chem Toxicol 47: 1378–1384. doi: 10.1016/j.fct.2009.03.016
    [54] Foley SA, Mulloy B, Tuohy MG, et al. (2011) An unfractionated fucoidan from Ascophyllum nodosum: Extraction, characterization, and apoptotic effects in vitro. J Nat Prod 74: 1851–1861. doi: 10.1021/np200124m
    [55] Jiang Z, Okimura T, Yokose T (2010) Effects of sulfated fucan, ascophyllan, from the brown Alga Ascophyllum nodosum on various cell lines: A comparative study on ascophyllan and fucoidan. J Biosci Bioeng 110: 113–117. doi: 10.1016/j.jbiosc.2010.01.007
    [56] Zhang Z, Kiichiro T, Hiroshi E, et al. (2011) Fucoidan extract induces apoptosis in MCF-7 cells via a mechanism involving the ROS-dependent JNK activation and mitochondria-mediated pathways. PLoS One 6: e27441. doi: 10.1371/journal.pone.0027441
    [57] Jiao G, Yu G, Zhang J, et al. (2011) Chemical structures and bioactivities of sulfated polysaccharides from marine algae. Mar Drugs 9: 196–223. doi: 10.3390/md9020196
    [58] Cumashi A, Ushakova NA, Preobrazhenskaya ME, et al. (2007) A comparative study of the anti-inflammatory, anticoagulant, antiangiogenic, and antiadhesive activities of nine different fucoidans from brown seaweeds. Glycobiology 17: 541–552. doi: 10.1093/glycob/cwm014
    [59] Hyun J, Kim S, Kang J, et al. (2009) Apoptosis inducing activity of fucoidan in HCT-15 colon carcinoma cells. Biol Pharm Bull 32: 1760–1764. doi: 10.1248/bpb.32.1760
    [60] Park HS, Kim GY, Nam TJ, et al. (2011) Antiproliferative activity of fucoidan was associated with the induction of apoptosis and autophagy in AGS human gastric cancer cells. J Food Sci 76: T77–T83. doi: 10.1111/j.1750-3841.2011.02099.x
    [61] Luo M, Shao B, Nie W, et al. (2015) Antitumor and Adjuvant Activity of λ-carrageenan by Stimulating Immune Response in Cancer Immunotherapy. Sci Rep 5: 11062. doi: 10.1038/srep11062
    [62] Jazzara M, Ghannam A, Soukkarieh C, et al. (2016) Anti-Proliferative Activity of λ-Carrageenan Through the Induction of Apoptosis in Human Breast Cancer Cells. Iran J Cancer Prev 9: e3836.
    [63] Yuan Y, Song J, Li X, et al. (2011) Enhanced immunostimulatory and antitumor activity of different derivatives of kappa-carrageenan oligosaccharides from Kappaphycus striatum. J Appl Phycol 23: 59–65. doi: 10.1007/s10811-010-9536-4
    [64] Fedorov SN, Ermakova SP, Zvyagintseva TN, et al. (2013) Anticancer and Cancer Preventive Properties of Marine Polysaccharides: Some Results and Prospects. Mar Drugs 11: 4876–4901. doi: 10.3390/md11124876
    [65] Yermak IM, Barabanova AO, Aminin DL, et al. (2012) Effects of structural peculiarities of carrageenans on their immunomodulatory and anticoagulant activities. Carbohydr Polym 87: 713–720. doi: 10.1016/j.carbpol.2011.08.053
    [66] Kalitnik AA, Anastyuk SD, Sokolova EV, et al. (2016) Oligosaccharides of k/β-carrageenan from the red alga Tichocarpus crinitus and their ability to induce interleukin 10. J Appl Phycol 28: 545–553. doi: 10.1007/s10811-015-0577-6
    [67] Thomson AW, Fowler EF (1981) Carrageenan: A review of its effects on the immune system. Agents Actions 11: 265–273. doi: 10.1007/BF01967625
    [68] Morais-Zani KD, Nunes FPB, Silva JBD, et al. (2013) The anti-inflammatory action of Bothrops jararaca snake antithrombin on acute inflammation induced by carrageenan in mice. Inflammation Res 62: 733–742. doi: 10.1007/s00011-013-0628-x
    [69] Tsuji R, Hoshino K, Noro Y, et al. (2003) Suppression of allergic reaction by λ-carrageenan: Toll-like receptor 4/MyD88-dependent and -independent modulation of immunity. Clin Exp Allergy 33: 249–258. doi: 10.1046/j.1365-2222.2003.01575.x
    [70] Garcia AM, Chaly ES (1996) Preliminary spherical agglomerates of water-soluble drug using natural polymer and cross-linking technique. J Controlled Release 40: 179–186. doi: 10.1016/0168-3659(95)00179-4
    [71] Schmidt AG, Wartewig S, Picker KM (2003) Potential of carrageenans to protect drugs from polymorphic transformation. Eur J Pharm Biopharm 56: 101–110. doi: 10.1016/S0939-6411(03)00037-7
    [72] Thommes M, Kleinebudde P (2006) Use of kappa-carrageenan as alternative pelletisation aid to microcrystalline cellulose in extrusion/spheronisation. I. Influence of type and fraction of filler. Eur J Pharm Biopharm 63: 59–67.
    [73] Hugerth AM (2001) Micropolarity and microviscosity of amitriptyline and dextran sulfate/carrageenan-amitriptyline systems: The nature of polyelectrolyte-drug complexes. J Pharm Sci 90: 1665–1677. doi: 10.1002/jps.1117
    [74] Patil RT, Speaker TJ (2000) Water-based microsphere delivery system for proteins. J Pharm Sci 89: 9–15. doi: 10.1002/(SICI)1520-6017(200001)89:1<9::AID-JPS2>3.0.CO;2-5
    [75] Yermak IM, Khotimchenko YS (2003) Chemical properties, biological activities and applications of carrageenan from red algae. Recent Adv Mar Biotechnol 9: 207–255.
    [76] Volod'ko AV, Davydova VN, Chusovitin E, et al. (2014) Soluble chitosan carrageenan polyelectrolyte complexes and their gastroprotective activity. Carbohydr Polym 101: 1087. doi: 10.1016/j.carbpol.2013.10.049
    [77] Lahaye M, Kaeffer B (1997) Seaweed dietary fibres: Structure, physico-chemical and biological properties relevent to intestinal physiology. Sci Aliment 17: 563–584.
    [78] Cummings JH, Mann JI, Nishida C, et al. (2009) Dietary fibre: An agreed definition. Lancet 373: 365–366. doi: 10.1016/S0140-6736(09)60117-3
    [79] Harris RE, Chlebowski RT, Jackson RD, et al. (2003) Breast cancer and nonsteroidal anti-inflammatory drugs: Prospective results from the Women's Health Initiative. Cancer Res 63: 6096–6101.
    [80] Stansbury, Jillian, SEAWEED, CHEWING GUM AND GERD. Ndnr Botanical Medicine, [Online] January 17, 2017. Available from: http://ndnr.com/botanical-medicine/seaweed-chewing-gum-and-gerd/#comments.
    [81] Greene ER, Huang S, Serhan CN, et al. (2011) Regulation of inflammation in cancer by eicosanoids. Prostaglandins Other Lipid Mediators 96: 27–36. doi: 10.1016/j.prostaglandins.2011.08.004
    [82] Coussens LM, Werb Z (2002) Inflammation and cancer. Nature 420: 860–867. doi: 10.1038/nature01322
    [83] Vakkila J, Lotze MT (2004) Inflammation and necrosis promote tumour growth. Nat Rev Immunol 4: 641–648. doi: 10.1038/nri1415
    [84] Ekbom A, Helmick C, Zack M, et al. (1990) Ulcerative colitis and colorectal cancer. N Engl J Med 323: 1228–1233. doi: 10.1056/NEJM199011013231802
    [85] Kulaylat MN, Dayton MT (2010) Ulcerative colitis and cancer. J Surg Oncol 101: 706–712. doi: 10.1002/jso.21505
    [86] Kalitnik AA, Marcov PA, Anastyuk SD, et al. (2015) Gelling polysaccharide from Chondrus armatus and its oligosaccharides: The structural peculiarities and anti-inflammatory. Carbohydr Polym 115: 768–775. doi: 10.1016/j.carbpol.2014.04.070
    [87] Sokolova EV, Karetin Y, Davydova VN, et al. (2016) Carrageenans effect on neutrophils alone and in combination with LPS in vitro. J Biomed Mater Res Part A 104: 1603–1609. doi: 10.1002/jbm.a.35693
    [88] Abdel-Latif MM, Duggan S, Reynolds JV, et al. (2009) Inflammation and esophageal carcinogenesis. Curr Opin Pharmacol 9: 396–404. doi: 10.1016/j.coph.2009.06.010
    [89] Hardikar S, Onstad L, Song X, et al. (2014) Inflammation and oxidative stress markers and esophageal adenocarcinoma incidence in a Barrett's esophagus cohort. Cancer Epidemiol Biomarkers Prev 23: 2393–2403. doi: 10.1158/1055-9965.EPI-14-0384
    [90] Wang Q, Hao J, Guan Q, et al. (2014) The Mediterranean diet and gastrointestinal cancers risk. Recent Pat Food Nutr Agric 6: 23–26. doi: 10.2174/2212798406666141024111945
    [91] Jessri M, Rashidkhani B, Hajizadeh B, et al. (2012) Adherence to Mediterranean-style dietary pattern and risk of esophageal squamous cell carcinoma: A case-control study in Iran. J Am Coll Nutr 31: 338–351. doi: 10.1080/07315724.2012.10720437
    [92] Caliari SR, Burdick JA (2016) A practical guide to hydrogels for cell culture. Nat Methods 13: 405–414. doi: 10.1038/nmeth.3839
    [93] Rybtsov S, Batsivari A, Bilotkach K, et al. (2014) Tracing the origin of the HSC hierarchy reveals an SCF-dependent, IL-3-independent CD43- embryonic precursor. Stem Cell Rep 3: 489–501. doi: 10.1016/j.stemcr.2014.07.009
    [94] Huang Q, Zou Y, Arno MC, et al. (2017) Hydrogel scaffolds for differentiation of adipose-derived stem cells. Chem Soc Rev 46: 6255–6275. doi: 10.1039/C6CS00052E
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