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For: Zhang JJ, Wu HS, Wang L, Tian Y, Zhang JH, Wu HL. Expression and significance of TLR4 and HIF-1α in pancreatic ductal adenocarcinoma. World J Gastroenterol 2010; 16(23): 2881-2888 [PMID: 20556833 DOI: 10.3748/wjg.v16.i23.2881]
URL: https://www.wjgnet.com/1007-9327/full/v16/i23/2881.htm
Number Citing Articles
1
Ashley Mansell, Brendan J. Jenkins. Dangerous liaisons between interleukin-6 cytokine and toll-like receptor families: A potent combination in inflammation and cancerCytokine & Growth Factor Reviews 2013; 24(3): 249 doi: 10.1016/j.cytogfr.2013.03.007
2
Elisa Barone, Alda Corrado, Federica Gemignani, Stefano Landi. Environmental risk factors for pancreatic cancer: an updateArchives of Toxicology 2016; 90(11): 2617 doi: 10.1007/s00204-016-1821-9
3
Lina Elsalem, Ahmad A Jum'ah, Mahmoud A Alfaqih, Osama Aloudat. <p>The Bacterial Microbiota of Gastrointestinal Cancers: Role in Cancer Pathogenesis and Therapeutic Perspectives</p>Clinical and Experimental Gastroenterology 2020; : 151 doi: 10.2147/CEG.S243337
4
Somaiyeh Malekghasemi, Jafar Majidi, Behzad Baradaran, Leili Aghebati‐Maleki. Prostate cancer cells modulate the differentiation of THP‐1 cells in response to etoposide and TLR agonists treatmentsCell Biology International 2020; 44(10): 2031 doi: 10.1002/cbin.11410
5
Sandeep Rajput, Lisa D. Volk-Draper, Sophia Ran. TLR4 Is a Novel Determinant of the Response to Paclitaxel in Breast CancerMolecular Cancer Therapeutics 2013; 12(8): 1676 doi: 10.1158/1535-7163.MCT-12-1019
6
Zhen Luo, Zhong‐Jie Yi, Zheng‐Lin Ou, Tong Han, Tao Wan, Yong‐Chang Tang, Zhi‐Chao Wang, Fei‐Zhou Huang. RELA/NEAT1/miR‐302a‐3p/RELA feedback loop modulates pancreatic ductal adenocarcinoma cell proliferation and migrationJournal of Cellular Physiology 2019; 234(4): 3583 doi: 10.1002/jcp.27039
7
Fabienne Guillaumond, Juan Lucio Iovanna, Sophie Vasseur. Pancreatic tumor cell metabolism: Focus on glycolysis and its connected metabolic pathwaysArchives of Biochemistry and Biophysics 2014; 545: 69 doi: 10.1016/j.abb.2013.12.019
8
Hai-ying Fu, Chun Li, Wei Yang, Xiao-dong Gai, Ting Jia, Yan-ming Lei, Yi Li. FOXP3 and TLR4 protein expression are correlated in non-small cell lung cancer: Implications for tumor progression and escapeActa Histochemica 2013; 115(2): 151 doi: 10.1016/j.acthis.2012.06.002
9
Pankti C. Balar, Vasso Apostolopoulos, Vivek P. Chavda. A new era of immune therapeutics for pancreatic cancer: Monoclonal antibodies paving the wayEuropean Journal of Pharmacology 2024; 969: 176451 doi: 10.1016/j.ejphar.2024.176451
10
Shipra Das, Beny Shapiro, Emily A. Vucic, Sandra Vogt, Dafna Bar-Sagi. Tumor Cell–Derived IL1β Promotes Desmoplasia and Immune Suppression in Pancreatic CancerCancer Research 2020; 80(5): 1088 doi: 10.1158/0008-5472.CAN-19-2080
11
Amirhossein Moslemizadeh, Mohammad Hadi Nematollahi, Sedigheh Amiresmaili, Sanaz Faramarz, Elham Jafari, Mohammad Khaksari, Nima Rezaei, Hamideh Bashiri, Reza Kheirandish. Combination therapy with interferon-gamma as a potential therapeutic medicine in rat's glioblastoma: A multi-mechanism evaluationLife Sciences 2022; 305: 120744 doi: 10.1016/j.lfs.2022.120744
12
Hanlin Yin, Ning Pu, Qiangda Chen, Jicheng Zhang, Guochao Zhao, Xuefeng Xu, Dansong Wang, Tiantao Kuang, Dayong Jin, Wenhui Lou, Wenchuan Wu. Gut-derived lipopolysaccharide remodels tumoral microenvironment and synergizes with PD-L1 checkpoint blockade via TLR4/MyD88/AKT/NF-κB pathway in pancreatic cancerCell Death & Disease 2021; 12(11) doi: 10.1038/s41419-021-04293-4
13
Ann H. Rosendahl, Chen Sun, DeQuan Wu, Roland Andersson. Polysaccharide-K (PSK) increases p21WAF/Cip1 and promotes apoptosis in pancreatic cancer cellsPancreatology 2012; 12(6): 467 doi: 10.1016/j.pan.2012.09.004
14
Bo Hao, Zhen Chen, Baochen Bi, Miaomei Yu, Shuang Yao, Yuehua Feng, Yang Yu, Lili Pan, Dongmei Di, Guanghua Luo, Xiaoying Zhang. Role of TLR4 as a prognostic factor for survival in various cancers: a meta-analysisOncotarget 2018; 9(16): 13088 doi: 10.18632/oncotarget.24178
15
Bin Zhao, Xiulong Niu, Suhui Huang, Jing Yang, Yiyi Wei, Xiujuan Wang, Junhong Wang, Yue Wang, Xiaoqin Guo, Ulises Urzua. TLR4 Agonist and Hypoxia Synergistically Promote the Formation of TLR4/NF-κB/HIF-1α Loop in Human Epithelial Ovarian CancerAnalytical Cellular Pathology 2022; 2022: 1 doi: 10.1155/2022/4201262
16
Chih‐Cheng Hsiao, Ying‐Hsien Kao, Shun‐Chen Huang, Jiin‐Haur Chuang. Toll‐like receptor‐4 agonist inhibits motility and invasion of hepatoblastoma HepG2 cells in vitroPediatric Blood & Cancer 2013; 60(2): 248 doi: 10.1002/pbc.24211
17
Sara Zanini, Serena Renzi, Antonina R. Limongi, Paolo Bellavite, Francesco Giovinazzo, Giovanna Bermano. A review of lifestyle and environment risk factors for pancreatic cancerEuropean Journal of Cancer 2021; 145: 53 doi: 10.1016/j.ejca.2020.11.040
18
Sabina Strapcova, Martina Takacova, Lucia Csaderova, Paola Martinelli, Lubomira Lukacikova, Viliam Gal, Juraj Kopacek, Eliska Svastova. Clinical and Pre-Clinical Evidence of Carbonic Anhydrase IX in Pancreatic Cancer and Its High Expression in Pre-Cancerous LesionsCancers 2020; 12(8): 2005 doi: 10.3390/cancers12082005
19
Linli Yao, Enci Mary Kan, Jia Lu, Aijun Hao, S Thameem Dheen, Charanjit Kaur, Eng-Ang Ling. Toll-like receptor 4 mediates microglial activation and production of inflammatory mediators in neonatal rat brain following hypoxia: role of TLR4 in hypoxic microgliaJournal of Neuroinflammation 2013; 10(1) doi: 10.1186/1742-2094-10-23
20
Anton G. Kutikhin, Arseniy E. Yuzhalin. Genomics of Pattern Recognition Receptors2013; : 1 doi: 10.1007/978-3-0348-0688-6_1
21
Sunhwa Kim, Michael Karin. Role of TLR2‐dependent inflammation in metastatic progressionAnnals of the New York Academy of Sciences 2011; 1217(1): 191 doi: 10.1111/j.1749-6632.2010.05882.x
22
Wei Ping, Wen-Yang Jiang, Wen-Shu Chen, Wei Sun, Xiang-Ning Fu. Expression and Significance of Hypoxia Inducible Factor-1α and Lysyl Oxidase in Non-small Cell Lung CancerAsian Pacific Journal of Cancer Prevention 2013; 14(6): 3613 doi: 10.7314/APJCP.2013.14.6.3613
23
Jianhui Liu, Dong Xu, Qingguang Wang, Datong Zheng, Xiuqin Jiang, Lijian Xu. LPS Induced miR-181a Promotes Pancreatic Cancer Cell Migration via Targeting PTEN and MAP2K4Digestive Diseases and Sciences 2014; 59(7): 1452 doi: 10.1007/s10620-014-3049-y
24
Daniel Delitto, Andrea E. Delitto, Bayli B. DiVita, Kien Pham, Song Han, Emily R. Hartlage, Brittney N. Newby, Michael H. Gerber, Kevin E. Behrns, Lyle L. Moldawer, Ryan M. Thomas, Thomas J. George, Todd M. Brusko, Clayton E. Mathews, Chen Liu, Jose G. Trevino, Steven J. Hughes, Shannon M. Wallet. Human Pancreatic Cancer Cells Induce a MyD88-Dependent Stromal Response to Promote a Tumor-Tolerant Immune MicroenvironmentCancer Research 2017; 77(3): 672 doi: 10.1158/0008-5472.CAN-16-1765
25
Murielle Mimeault, Surinder K. Batra. Hypoxia‐inducing factors as master regulators of stemness properties and altered metabolism of cancer‐ and metastasis‐initiating cellsJournal of Cellular and Molecular Medicine 2013; 17(1): 30 doi: 10.1111/jcmm.12004
26
Edward J. Kim, Diane M. Simeone. Advances in pancreatic cancerCurrent Opinion in Gastroenterology 2011; 27(5): 460 doi: 10.1097/MOG.0b013e328349e31f
27
Matteo Santoni, Kalliopi Andrikou, Valeria Sotte, Alessandro Bittoni, Andrea Lanese, Chiara Pellei, Francesco Piva, Alessandro Conti, Massimo Nabissi, Giorgio Santoni, Stefano Cascinu. Toll like receptors and pancreatic diseases: From a pathogenetic mechanism to a therapeutic targetCancer Treatment Reviews 2015; 41(7): 569 doi: 10.1016/j.ctrv.2015.04.004
28
Miao-Yan Wei, Si Shi, Chen Liang, Qing-Cai Meng, Jie Hua, Yi-Yin Zhang, Jiang Liu, Bo Zhang, Jin Xu, Xian-Jun Yu. The microbiota and microbiome in pancreatic cancer: more influential than expectedMolecular Cancer 2019; 18(1) doi: 10.1186/s12943-019-1008-0
29
Yiyi Zhang, Nie Tang, Hui Zhou, Ying Zhu. The role of microbial metabolites in endocrine tumorigenesis: From the mechanistic insights to potential therapeutic biomarkersBiomedicine & Pharmacotherapy 2024; 172: 116218 doi: 10.1016/j.biopha.2024.116218
30
Mira A Lanki, Hanna E Seppänen, Harri K Mustonen, Camilla Böckelman, Anne T Juuti, Jaana K Hagström, Caj H Haglund. Toll-like receptor 2 and Toll-like receptor 4 predict favorable prognosis in local pancreatic cancerTumor Biology 2018; 40(9): 101042831880118 doi: 10.1177/1010428318801188
31
Mousami Srivastava, Pankaj Khurana, Ragumani Sugadev. Lung Cancer Signature Biomarkers: tissue specific semantic similarity based clustering of Digital Differential Display (DDD) dataBMC Research Notes 2012; 5(1) doi: 10.1186/1756-0500-5-617
32
Elisa Perez-Moreno, Claudia Oyanadel, Adely de la Peña, Ronny Hernández, Francisca Pérez-Molina, Claudia Metz, Alfonso González, Andrea Soza. Galectins in epithelial-mesenchymal transition: roles and mechanisms contributing to tissue repair, fibrosis and cancer metastasisBiological Research 2024; 57(1) doi: 10.1186/s40659-024-00490-5
33
Joni Leppänen, Olli Helminen, Heikki Huhta, Joonas H. Kauppila, Joel Isohookana, Kirsi-Maria Haapasaari, Seppo Parkkila, Juha Saarnio, Petri P. Lehenkari, Tuomo J. Karttunen. Weak HIF-1alpha expression indicates poor prognosis in resectable pancreatic ductal adenocarcinomaWorld Journal of Surgical Oncology 2018; 16(1) doi: 10.1186/s12957-018-1432-4
34
Makena J. Binker-Cosen, Daniel Richards, Brenda Oliver, Herbert Y. Gaisano, Marcelo G. Binker, Laura I. Cosen-Binker. Palmitic acid increases invasiveness of pancreatic cancer cells AsPC-1 through TLR4/ROS/NF-κB/MMP-9 signaling pathwayBiochemical and Biophysical Research Communications 2017; 484(1): 152 doi: 10.1016/j.bbrc.2017.01.051
35
Sophia Ran, Nihit Bhattarai, Radhika Patel, Lisa Volk-Draper. Translational Studies on Inflammation2020;  doi: 10.5772/intechopen.85195
36
Lisa A. Ridnour, Robert Y.S. Cheng, Christopher H. Switzer, Julie L. Heinecke, Stefan Ambs, Sharon Glynn, Howard A. Young, Giorgio Trinchieri, David A. Wink. Molecular Pathways: Toll-like Receptors in the Tumor Microenvironment—Poor Prognosis or New Therapeutic OpportunityClinical Cancer Research 2013; 19(6): 1340 doi: 10.1158/1078-0432.CCR-12-0408
37
Zhou Chen, Shaofeng Zhang, Shi Dong, Hao Xu, Wence Zhou. Association of the Microbiota and Pancreatic Cancer: Opportunities and LimitationsFrontiers in Immunology 2022; 13 doi: 10.3389/fimmu.2022.844401
38
D. S. Michaud. Role of bacterial infections in pancreatic cancerCarcinogenesis 2013; 34(10): 2193 doi: 10.1093/carcin/bgt249
39
Tandrima Mitra, Soumya S. Mahapatra, Barnalee Mishra, Venketesh K. Panda, Diksha Malhotra, Anusuya Roychowdhury, Gopal C. Kundu. Hypoxia in Cancer: Significance and Impact on Cancer Therapy2023; : 1 doi: 10.1007/978-981-99-0313-9_1
40
Yunliang Sun, Congshan Wu, Jianxia Ma, Yu Yang, Xiaohua Man, Hongyu Wu, Shude Li. Toll-like receptor 4 promotes angiogenesis in pancreatic cancer via PI3K/AKT signalingExperimental Cell Research 2016; 347(2): 274 doi: 10.1016/j.yexcr.2016.07.009
41
Long-Yun Ye, Qi Zhang, Xue-Li Bai, Prasoon Pankaj, Qi-Da Hu, Ting-Bo Liang. Hypoxia-inducible factor 1α expression and its clinical significance in pancreatic cancer: A meta-analysisPancreatology 2014; 14(5): 391 doi: 10.1016/j.pan.2014.06.008
42
Dajia Liu, Anne Steins, Remy Klaassen, Amber P. van der Zalm, Roel J. Bennink, Geertjan van Tienhoven, Marc G. Besselink, Maarten F. Bijlsma, Hanneke W. M. van Laarhoven. Soluble Compounds Released by Hypoxic Stroma Confer Invasive Properties to Pancreatic Ductal AdenocarcinomaBiomedicines 2020; 8(11): 444 doi: 10.3390/biomedicines8110444
43
Xinming Jing, Fengming Yang, Chuchu Shao, Ke Wei, Mengyan Xie, Hua Shen, Yongqian Shu. Role of hypoxia in cancer therapy by regulating the tumor microenvironmentMolecular Cancer 2019; 18(1) doi: 10.1186/s12943-019-1089-9
44
Ki Hyung Kim, Moo Sung Jo, Dong Soo Suh, Man Soo Yoon, Dong Hun Shin, Jeong Hee Lee, Kyung Un Choi. Expression and significance of the TLR4/MyD88 signaling pathway in ovarian epithelial cancersWorld Journal of Surgical Oncology 2012; 10(1) doi: 10.1186/1477-7819-10-193
45
Zhichao Liu, Hong Fang, William Slikker, Weida Tong. Potential Reuse of Oncology Drugs in the Treatment of Rare DiseasesTrends in Pharmacological Sciences 2016; 37(10): 843 doi: 10.1016/j.tips.2016.06.010
46
Zhou Chen, Defeng Guan, Zhengfeng Wang, Xin Li, Shi Dong, Junjun Huang, Wence Zhou. Microbiota in cancer: molecular mechanisms and therapeutic interventionsMedComm 2023; 4(6) doi: 10.1002/mco2.417
47
Ling Zhou, Lianwen Qi, Lifeng Jiang, Ping Zhou, Jiang Ma, Xiaojun Xu, Ping Li. Antitumor Activity of Gemcitabine Can Be Potentiated in Pancreatic Cancer through Modulation of TLR4/NF-κB signaling by 6-ShogaolThe AAPS Journal 2014; 16(2): 246 doi: 10.1208/s12248-013-9558-3
48
I-Ting Chen, An-Chieh Cheng, Yi-Ting Liu, Chieh Yan, Yi-Chen Cheng, Chiung-Fang Chang, Ping-Hui Tseng. Persistent TLR4 Activation Promotes Hepatocellular Carcinoma Growth through Positive Feedback Regulation by LIN28A/Let-7g miRNAInternational Journal of Molecular Sciences 2022; 23(15): 8419 doi: 10.3390/ijms23158419
49
Guanglei Fan, Jingli Bo, Renming Wan, Mingya Peng, Yufen Luan, Minbin Deng, Longbao Xu. The Effect of Lentiviral Vector-Mediated RNA Interference Targeting Hypoxia-Inducible Factor 1α on the Uptake of Fluorodeoxyglucose (18F) in the Human Pancreatic Cancer Cell Line, Patu8988Cancer Biotherapy and Radiopharmaceuticals 2015; 30(4): 160 doi: 10.1089/cbr.2014.1700
50
Anton G. Kutikhin. Association of polymorphisms in TLR genes and in genes of the Toll-like receptor signaling pathway with cancer riskHuman Immunology 2011; 72(11): 1095 doi: 10.1016/j.humimm.2011.07.307
51
Lisa Volk-Draper, Kelly Hall, Caitlin Griggs, Sandeep Rajput, Pascaline Kohio, David DeNardo, Sophia Ran. Paclitaxel Therapy Promotes Breast Cancer Metastasis in a TLR4-Dependent MannerCancer Research 2014; 74(19): 5421 doi: 10.1158/0008-5472.CAN-14-0067
52
Ga-Bin Park, Jee-Yeong Jeong, Daejin Kim. GLUT5 regulation by AKT1/3-miR-125b-5p downregulation induces migratory activity and drug resistance in TLR-modified colorectal cancer cellsCarcinogenesis 2020; 41(10): 1329 doi: 10.1093/carcin/bgaa074
53
Anna Maria Nurmi, Jaana Hagström, Harri Mustonen, Hanna Seppänen, Caj Haglund, Girijesh Kumar Patel. The expression and prognostic value of toll-like receptors (TLRs) in pancreatic cancer patients treated with neoadjuvant therapyPLOS ONE 2022; 17(5): e0267792 doi: 10.1371/journal.pone.0267792
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E. Marks, C. Naudin, G. Nolan, B.J. Goggins, G. Burns, S.W. Mateer, J.K. Latimore, K. Minahan, M. Plank, P.S. Foster, R. Callister, M. Veysey, M.M. Walker, N.J. Talley, G. Radford-Smith, S. Keely. Regulation of IL-12p40 by HIF controls Th1/Th17 responses to prevent mucosal inflammationMucosal Immunology 2017; 10(5): 1224 doi: 10.1038/mi.2016.135
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Xin Wei, Chunlei Mei, Xixi Li, Yingjun Xie. The Unique Microbiome and Immunity in Pancreatic CancerPancreas 2021; 50(2): 119 doi: 10.1097/MPA.0000000000001744
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Tongshuo Zhang, Jing Yang, Yang Sun, Jiangnan Song, Dandan Gao, Suhui Huang, Aibo Pang, Jianhui Zhang, Junhong Wang, Yue Wang, Yanqiu Li, Silvia Cantara. Interleukin-6 and Hypoxia Synergistically Promote EMT-Mediated Invasion in Epithelial Ovarian Cancer via the IL-6/STAT3/HIF-1α Feedback LoopAnalytical Cellular Pathology 2023; 2023: 1 doi: 10.1155/2023/8334881
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Prasanna Srinivasan Ramalingam, Sivakumar Arumugam. Reverse vaccinology and immunoinformatics approaches to design multi-epitope based vaccine against oncogenic KRASMedical Oncology 2023; 40(10) doi: 10.1007/s12032-023-02160-0
58
Mitsuru Sugimoto, Kazumichi Abe, Tadayuki Takagi, Rei Suzuki, Naoki Konno, Hiroyuki Asama, Yuki Sato, Hiroki Irie, Ko Watanabe, Jun Nakamura, Hitomi Kikuchi, Mika Takasumi, Minami Hashimoto, Tsunetaka Kato, Ryoichiro Kobashi, Takuto Hikichi, Hiromasa Ohira. Dysbiosis of the duodenal microbiota as a diagnostic marker for pancreaticobiliary cancerWorld Journal of Gastrointestinal Oncology 2021; 13(12): 2088-2100 doi: 10.4251/wjgo.v13.i12.2088
59
Mahesh Chandra Patra, Masaud Shah, Sangdun Choi. Toll-like receptor-induced cytokines as immunotherapeutic targets in cancers and autoimmune diseasesSeminars in Cancer Biology 2020; 64: 61 doi: 10.1016/j.semcancer.2019.05.002
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Goutam Chowdhury, Dharanidharan Ramamurthy. Human Microbiome2022; : 73 doi: 10.1007/978-981-16-7672-7_4
61
Joni Leppänen, Olli Helminen, Heikki Huhta, Joonas H. Kauppila, Joel Isohookana, Kirsi-Maria Haapasaari, Petri Lehenkari, Juha Saarnio, Tuomo J. Karttunen. High toll-like receptor (TLR) 9 expression is associated with better prognosis in surgically treated pancreatic cancer patientsVirchows Archiv 2017; 470(4): 401 doi: 10.1007/s00428-017-2087-1
62
Katharina Beyer, Lars Ivo Partecke, Felicitas Roetz, Herbert Fluhr, Frank Ulrich Weiss, Claus-Dieter Heidecke, Wolfram von Bernstorff. LPS promotes resistance to TRAIL-induced apoptosis in pancreatic cancerInfectious Agents and Cancer 2017; 12(1) doi: 10.1186/s13027-017-0139-4
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Jaroslaw Daniluk, Urszula Daniluk, Pawel Rogalski, Andrzej Dabrowski, Agnieszka Swidnicka-Siergiejko. Microbiome—Friend or Foe of Pancreatic Cancer?Journal of Clinical Medicine 2021; 10(23): 5624 doi: 10.3390/jcm10235624
64
Marion Dajon, Kristina Iribarren, Isabelle Cremer. Toll-like receptor stimulation in cancer: A pro- and anti-tumor double-edged swordImmunobiology 2017; 222(1): 89 doi: 10.1016/j.imbio.2016.06.009
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Shaherin Basith, Balachandran Manavalan, Tae Hyeon Yoo, Sang Geon Kim, Sangdun Choi. Roles of toll-like receptors in Cancer: A double-edged sword for defense and offenseArchives of Pharmacal Research 2012; 35(8): 1297 doi: 10.1007/s12272-012-0802-7
66
Qian Zhang, Jun Dan, Shuang Meng, Yingjie Li, Jing Li. TLR4 inhibited autophagy by modulating PI3K/AKT/mTOR signaling pathway in Gastric cancer cell linesGene 2023; 876: 147520 doi: 10.1016/j.gene.2023.147520
67
Shrabon Hasnat, Roosa Hujanen, Bright I. Nwaru, Tuula Salo, Abdelhakim Salem. The Prognostic Value of Toll-Like Receptors in Head and Neck Squamous Cell Carcinoma: A Systematic Review and Meta-AnalysisInternational Journal of Molecular Sciences 2020; 21(19): 7255 doi: 10.3390/ijms21197255
68
Huan Yang, Bo Wang, Tao Wang, Longjiang Xu, Chunyan He, Huiyan Wen, Jie Yan, Honghong Su, Xueming Zhu, Kottarappat N. Dileepan. Toll-Like Receptor 4 Prompts Human Breast Cancer Cells Invasiveness via Lipopolysaccharide Stimulation and Is Overexpressed in Patients with Lymph Node MetastasisPLoS ONE 2014; 9(10): e109980 doi: 10.1371/journal.pone.0109980
69
Kaka Renaldi, Marcellus Simadibrata, Nur Rahadiani, Diah Rini Handjari, Alida Roswita Harahap, Kuntjoro Harimurti, Nasrul Zubir, Lianda Siregar, Imelda Maria Loho, Evlina Suzanna, Bonita Prawirodihardjo, Heriawaty Hidajat, Budi Widodo, Alphania Rahniayu, Renaningtyas Tambun, Andy William, Dadang Makmun. The Expressions of NF−κB, COX−2, Sp1, and c−Jun in Pancreatic Ductal Adenocarcinoma and Their Associations with Patient SurvivalPathophysiology 2023; 30(2): 92 doi: 10.3390/pathophysiology30020009