Zhe Sheng Chen

Summary

Affiliation: St. John's University
Country: USA

Publications

  1. ncbi Overexpression of P-glycoprotein induces acquired resistance to imatinib in chronic myelogenous leukemia cells
    Xing Xiang Peng
    Department of Pharmaceutical Sciences, St John s University, Queens, NY 11439, USA
    Chin J Cancer 31:110-8. 2012
  2. ncbi Multidrug resistance proteins (MRPs/ABCCs) in cancer chemotherapy and genetic diseases
    Zhe Sheng Chen
    Department of Pharmaceutical Sciences, College of Pharmacy and Allied Health Professions, St John s University, Queens, NY 11439, USA
    FEBS J 278:3226-45. 2011
  3. ncbi Erlotinib (Tarceva, OSI-774) antagonizes ATP-binding cassette subfamily B member 1 and ATP-binding cassette subfamily G member 2-mediated drug resistance
    Zhi Shi
    Department of Pharmaceutical Sciences, College of Pharmacy and Allied Health Professions, St John s University, Jamaica, New York 11439, USA
    Cancer Res 67:11012-20. 2007
  4. ncbi OSI-930 analogues as novel reversal agents for ABCG2-mediated multidrug resistance
    Ye Hong Kuang
    Department of Pharmaceutical Sciences, College of Pharmacy and Allied Health Professions, St John s University, Queens, NY 11439, USA
    Biochem Pharmacol 84:766-74. 2012
  5. ncbi Sipholenol A, a marine-derived sipholane triterpene, potently reverses P-glycoprotein (ABCB1)-mediated multidrug resistance in cancer cells
    Zhi Shi
    Department of Pharmaceutical Sciences, College of Pharmacy and Allied Health Professions, St John s University, Jamaica, NY 11439, USA
    Cancer Sci 98:1373-80. 2007
  6. ncbi Imatinib and nilotinib reverse multidrug resistance in cancer cells by inhibiting the efflux activity of the MRP7 (ABCC10)
    Tong Shen
    Department of Pharmaceutical Sciences, College of Pharmacy and Allied Health Professions, St John s University, Queens, New York, United States of America
    PLoS ONE 4:e7520. 2009
  7. ncbi Sildenafil reverses ABCB1- and ABCG2-mediated chemotherapeutic drug resistance
    Zhi Shi
    Department of Pharmaceutical Sciences, College of Pharmacy and Allied Health Professions, St John s University, Queens, New York 10016, USA
    Cancer Res 71:3029-41. 2011
  8. ncbi The epidermal growth factor tyrosine kinase inhibitor AG1478 and erlotinib reverse ABCG2-mediated drug resistance
    Zhi Shi
    Department of Pharmaceutical Sciences, St John s University, Jamaica, NY 11439, USA
    Oncol Rep 21:483-9. 2009
  9. ncbi Nilotinib potentiates anticancer drug sensitivity in murine ABCB1-, ABCG2-, and ABCC10-multidrug resistance xenograft models
    Amit K Tiwari
    Department of Pharmaceutical Sciences, College of Pharmacy and Health Sciences, St John s University, Queens, NY 11439, USA
    Cancer Lett 328:307-17. 2013
  10. ncbi Lapatinib and erlotinib are potent reversal agents for MRP7 (ABCC10)-mediated multidrug resistance
    Ye Hong Kuang
    Department of Pharmaceutical Sciences, College of Pharmacy and Allied Health Professions, St John s University, Queens, NY 11439, USA
    Biochem Pharmacol 79:154-61. 2010

Collaborators

  • Xiang Chen
  • Tanaji T Talele
  • Susan E Bates
  • Liwu Fu
  • Gary D Kruh
  • Dong Hua Yang
  • Tatsuhiko Furukawa
  • Vijaya L Damaraju
  • Shin ichi Akiyama
  • Amit K Tiwari
  • Zhi Shi
  • Kamlesh Sodani
  • Yue Li Sun
  • Ye Hong Kuang
  • Xing Xiang Peng
  • Ioana Abraham
  • Suresh V Ambudkar
  • Atish Patel
  • Charles R Ashby
  • Tong Shen
  • Satyakam Singh
  • Chun Ling Dai
  • Jun Jiang Chen
  • Robert W Robey
  • Ying Zhou
  • In Wha Kim
  • Wen Qi Jiang
  • Zhi jie Xiao
  • Jay P Patel
  • Pei Rong Ding
  • Xin An
  • Khalid El Sayed
  • Elizabeth Hopper-Borge
  • Suneet Shukla
  • Xing-Xiang Peng
  • Priyank Kumar
  • Si dong Chen
  • Rishil J Kathawala
  • Vijaya L Korlipara
  • Chung Pu Wu
  • Jeferson W K K Lee
  • Hsiang Chun Wu
  • Smitaben Parmar
  • Xiao Cong Huang
  • Sandeep Jain
  • Qiu Sheng Si
  • In-Wha Kim
  • Amal Kaddoumi
  • James M Gallo
  • Alaa H Abuznait
  • Kang Chen
  • Yang Lu Chen
  • Li Qiu Liao
  • Kelvin Zheng
  • Huiqin Guo
  • Saraubh G Vispute
  • Shinobu Ohnuma
  • Xingxiang Peng
  • Atish S Patel
  • Qi Si Lu
  • Yibo Sun
  • Mohammad A Khanfar
  • Yehong Kuang
  • Yu Lei
  • Curtis S Goldblatt
  • Jiangyong Ouyang
  • Yang Min Chen
  • Si Rong Wang
  • Angel Chen
  • Yining Shao
  • Feiyang Zang
  • Carol E Cass
  • Hsiang-Chun Wu
  • Xiao-Cong Huang
  • Amit Tiwari
  • Diaa T A Youssef
  • Qiu-Sheng Si

Detail Information

Publications27

  1. ncbi Overexpression of P-glycoprotein induces acquired resistance to imatinib in chronic myelogenous leukemia cells
    Xing Xiang Peng
    Department of Pharmaceutical Sciences, St John s University, Queens, NY 11439, USA
    Chin J Cancer 31:110-8. 2012
    ..These data suggest that the overexpression of P-gp may play a crucial role in acquired resistance to imatinib in CML K562-imatinib cells...
  2. ncbi Multidrug resistance proteins (MRPs/ABCCs) in cancer chemotherapy and genetic diseases
    Zhe Sheng Chen
    Department of Pharmaceutical Sciences, College of Pharmacy and Allied Health Professions, St John s University, Queens, NY 11439, USA
    FEBS J 278:3226-45. 2011
    ..The mutations in MRP2/ABCC2 leading to conjugated hyperbilirubinemia (Dubin-Johnson syndrome) and in MRP6/ABCC6 leading to the connective tissue disorder Pseudoxanthoma elasticum are also discussed...
  3. ncbi Erlotinib (Tarceva, OSI-774) antagonizes ATP-binding cassette subfamily B member 1 and ATP-binding cassette subfamily G member 2-mediated drug resistance
    Zhi Shi
    Department of Pharmaceutical Sciences, College of Pharmacy and Allied Health Professions, St John s University, Jamaica, New York 11439, USA
    Cancer Res 67:11012-20. 2007
    ..These findings may be useful for cancer combinational therapy with erlotinib in the clinic...
  4. ncbi OSI-930 analogues as novel reversal agents for ABCG2-mediated multidrug resistance
    Ye Hong Kuang
    Department of Pharmaceutical Sciences, College of Pharmacy and Allied Health Professions, St John s University, Queens, NY 11439, USA
    Biochem Pharmacol 84:766-74. 2012
    ..Thus VKJP1 and VKJP3 represent a new class of drugs for reducing MDR in ABCG2 over-expressing tumors...
  5. ncbi Sipholenol A, a marine-derived sipholane triterpene, potently reverses P-glycoprotein (ABCB1)-mediated multidrug resistance in cancer cells
    Zhi Shi
    Department of Pharmaceutical Sciences, College of Pharmacy and Allied Health Professions, St John s University, Jamaica, NY 11439, USA
    Cancer Sci 98:1373-80. 2007
    ....
  6. ncbi Imatinib and nilotinib reverse multidrug resistance in cancer cells by inhibiting the efflux activity of the MRP7 (ABCC10)
    Tong Shen
    Department of Pharmaceutical Sciences, College of Pharmacy and Allied Health Professions, St John s University, Queens, New York, United States of America
    PLoS ONE 4:e7520. 2009
    ..These findings suggest that imatinib or nilotinib, in combination with other antineoplastic drugs, may be useful in the treatment of certain resistant cancers...
  7. ncbi Sildenafil reverses ABCB1- and ABCG2-mediated chemotherapeutic drug resistance
    Zhi Shi
    Department of Pharmaceutical Sciences, College of Pharmacy and Allied Health Professions, St John s University, Queens, New York 10016, USA
    Cancer Res 71:3029-41. 2011
    ..Our findings suggest a possible strategy to enhance the distribution and potentially the activity of anticancer drugs by jointly using a clinically approved drug with known side effects and drug-drug interactions...
  8. ncbi The epidermal growth factor tyrosine kinase inhibitor AG1478 and erlotinib reverse ABCG2-mediated drug resistance
    Zhi Shi
    Department of Pharmaceutical Sciences, St John s University, Jamaica, NY 11439, USA
    Oncol Rep 21:483-9. 2009
    ..These results will be useful in the development of novel and more effective EGFR TKIs as well as the development of combinational chemotherapeutic strategies...
  9. ncbi Nilotinib potentiates anticancer drug sensitivity in murine ABCB1-, ABCG2-, and ABCC10-multidrug resistance xenograft models
    Amit K Tiwari
    Department of Pharmaceutical Sciences, College of Pharmacy and Health Sciences, St John s University, Queens, NY 11439, USA
    Cancer Lett 328:307-17. 2013
    ..The beneficial actions of nilotinib warrant consideration as viable combinations in the clinic with agents that suffer from MDR-mediated insensitivity...
  10. ncbi Lapatinib and erlotinib are potent reversal agents for MRP7 (ABCC10)-mediated multidrug resistance
    Ye Hong Kuang
    Department of Pharmaceutical Sciences, College of Pharmacy and Allied Health Professions, St John s University, Queens, NY 11439, USA
    Biochem Pharmacol 79:154-61. 2010
    ....
  11. ncbi Marine sponge-derived sipholane triterpenoids reverse P-glycoprotein (ABCB1)-mediated multidrug resistance in cancer cells
    Ioana Abraham
    Department of Pharmaceutical Sciences, College of Pharmacy and Allied Health Professions, St John s University, Jamaica, NY 11439, USA
    Biochem Pharmacol 80:1497-506. 2010
    ..In conclusion, sipholane triterpenoids efficiently inhibit the function of P-gp through direct interactions and may represent potential reversal agents for the treatment of MDR...
  12. ncbi GW583340 and GW2974, human EGFR and HER-2 inhibitors, reverse ABCG2- and ABCB1-mediated drug resistance
    Kamlesh Sodani
    Department of Pharmaceutical Sciences, College of Pharmacy and Allied Health Professions, St John s University, Queens, NY 11439, USA
    Biochem Pharmacol 83:1613-22. 2012
    ..These findings may be useful in developing combination therapy for cancer treatment with EGFR TKIs...
  13. ncbi Up-regulation of MRP4 and down-regulation of influx transporters in human leukemic cells with acquired resistance to 6-mercaptopurine
    Xing Xiang Peng
    Department of Pharmaceutical Sciences, College of Pharmacy and Allied Health Professions, St John s University, Jamaica, NY 11439, United States
    Leuk Res 32:799-809. 2008
    ..Taken together these results showed that up-regulation of MRP4 and down-regulation of influx transporters played a major role in 6-MP resistance of CEM-MP5 cells...
  14. ncbi The phosphodiesterase-5 inhibitor vardenafil is a potent inhibitor of ABCB1/P-glycoprotein transporter
    Pei Rong Ding
    Department of Pharmaceutical Sciences, College of Pharmacy and Allied Health Professions, St John s University, Jamaica, New York, United States of America
    PLoS ONE 6:e19329. 2011
    ..Overall, our results suggest that vardenafil reverses ABCB1-mediated MDR by directly blocking the drug efflux function of ABCB1...
  15. ncbi Reversal of MRP7 (ABCC10)-mediated multidrug resistance by tariquidar
    Yue Li Sun
    State Key Laboratory of Oncology in South China, Guangzhou, Guangdong, People s Republic of China
    PLoS ONE 8:e55576. 2013
    ....
  16. ncbi Zafirlukast antagonizes ATP-binding cassette subfamily G member 2-mediated multidrug resistance
    Yue Li Sun
    Department of Pharmaceutical Sciences, College of Pharmacy and Allied Health Professionals, St John s University, Queens, New York, USA
    Anticancer Drugs 23:865-73. 2012
    ..Our findings suggest a possible strategy to potentially enhance the activity of anticancer drugs using a clinically approved drug with known side effects and drug-drug interactions...
  17. ncbi PDE5 inhibitors, sildenafil and vardenafil, reverse multidrug resistance by inhibiting the efflux function of multidrug resistance protein 7 (ATP-binding Cassette C10) transporter
    Jun Jiang Chen
    Department of Pharmaceutical Sciences, College of Pharmacy and Allied Health Professions, St John s University, Jamaica, New York, USA
    Cancer Sci 103:1531-7. 2012
    ..Our findings indicate a potentially novel use of PDE5 inhibitors as an adjuvant chemotherapeutic agent in clinical practice...
  18. ncbi Roles of sildenafil in enhancing drug sensitivity in cancer
    Zhi Shi
    Department of Pharmaceutical Sciences, College of Pharmacy and Allied Health Professions, St John s University, Queens, New York, USA
    Cancer Res 71:3735-8. 2011
    ..Emerging evidence indicates that sildenafil and other phosphodiesterase type 5 inhibitors may enhance the sensitivity of certain types of cancer to standard chemotherapeutic drugs...
  19. ncbi BCR-ABL tyrosine kinase inhibitors in the treatment of Philadelphia chromosome positive chronic myeloid leukemia: a review
    Xin An
    Department of Pharmaceutical Sciences, College of Pharmacy and Allied Health Professions, St John s University, 8000 Utopia Parkway, Jamaica, NY 11439, USA
    Leuk Res 34:1255-68. 2010
    ..Here, we present an overview about the current treatment of Ph+ CML patients with the TKIs and the obstacles to successful treatment with these drugs...
  20. ncbi Revisiting the ABCs of multidrug resistance in cancer chemotherapy
    Amit K Tiwari
    Department of Pharmaceutical Sciences, College of Pharmacy and Allied Health Professions, St John s University, Queens, NY 11439, USA
    Curr Pharm Biotechnol 12:570-94. 2011
    ..This review briefly discusses the current knowledge regarding the clinical involvement of ABC transporters in MDR to antineoplastic drugs and highlights approaches undertaken so far to overcome ABC transporter-mediated MDR in cancer...
  21. ncbi Inhibiting the function of ABCB1 and ABCG2 by the EGFR tyrosine kinase inhibitor AG1478
    Zhi Shi
    Department of Pharmaceutical Sciences, College of Pharmacy and Allied Health Professions, St John s University, Jamaica, NY 11439, USA
    Biochem Pharmacol 77:781-93. 2009
    ..Our findings provide valuable contributions to the development of safer and more effective EGFR TKIs for use as anticancer agents in the clinic...
  22. ncbi Cepharanthine is a potent reversal agent for MRP7(ABCC10)-mediated multidrug resistance
    Ying Zhou
    Department of Pharmaceutical Sciences, College of Pharmacy and Allied Health Professions, St John s University, Jamaica, NY, USA
    Biochem Pharmacol 77:993-1001. 2009
    ..E(2)17betaG transport was competitively inhibited by cepharanthine with a K(i) value of 4.86microM. These findings indicate that cepharanthine reverses MRP7-mediated resistance to paclitaxel in a competitive manner...
  23. ncbi Role of ABC transporters in cancer chemotherapy
    Yue Li Sun
    Department of Pharmaceutical Sciences, St John s University, Jamaica, NY 11439, USA
    Chin J Cancer 31:51-7. 2012
    ..Modulators of ABC transporters have the potential to augment the efficacy of anticancer drugs. This editorial highlights some major findings related to ABC transporters and current strategies to overcome MDR...
  24. ncbi Multidrug resistance associated proteins in multidrug resistance
    Kamlesh Sodani
    Department of Pharmaceutical Sciences, St John s University, Queens, NY 11439, USA
    Chin J Cancer 31:58-72. 2012
    ..This review focuses mainly on the physiological functions, cellular resistance characteristics, and probable in vivo role of MRP1 to MRP9...
  25. ncbi Inhibition of c-Kit, VEGFR-2 (KDR), and ABCG2 by analogues of OSI-930
    Jay P Patel
    Department of Pharmaceutical Sciences, College of Pharmacy and Allied Health Professions, St John s University, Queens, NY 11439, USA
    Bioorg Med Chem Lett 21:6495-9. 2011
    ..Nitropyridyl derivative 5 and o-nitrophenyl derivative 7 exhibited complete inhibition of the ABCG2 pump with IC(50) values of 13.67μM and 16.67μM, respectively...
  26. ncbi Current status on marine products with reversal effect on cancer multidrug resistance
    Ioana Abraham
    Department of Pharmaceutical Sciences, College of Pharmacy and Health Sciences, St John s University, Queens, NY 11439, USA
    Mar Drugs 10:2312-21. 2012
    ..This review highlights several marine natural products with reversal effect on multidrug resistance in cancer, including agosterol A, ecteinascidin 743, sipholane triterpenoids, bryostatin 1, and welwitindolinones...
  27. ncbi Nilotinib (AMN107, Tasigna) reverses multidrug resistance by inhibiting the activity of the ABCB1/Pgp and ABCG2/BCRP/MXR transporters
    Amit K Tiwari
    Department of Pharmaceutical Sciences, College of Pharmacy and Allied Health Professions, St John s University, 8000 Utopia Parkway, Jamaica, NY 11439, USA
    Biochem Pharmacol 78:153-61. 2009
    ..Also, these findings may be useful in clinical practice for cancer combination therapy with nilotinib...