YANG Cuixia  

  • Doctoral Supervisor, Professor
  • Department: Laboratory Medicine
  • Research Area: Clinical Diagnostics
  • Research Interests: Mechanisms of  metastasis and  endocrine resistance in breast cancer
  • Contact: dr.steven@163.com
  • Deputy Director, Clinical Laboratory, Shanghai Sixth People's Hospital, 2022  
  • PhD from Shanghai Jiao Tong University School of Medicine, 2014
  • Visiting Scholar, University of Miami School of Medicine, 2012                                                                      
  • MD from Qingdao University School of Medicine, 2002                                                                                                                       
  • Deputy Director, Department of  Clinical Laboratory, Shanghai Sixth People's Hospital
  • Member of the Laboratory Medicine Branch of Shanghai Medical Association
  • Representative of Shanghai Science and Technology Association
  • Member of the Committee of Laboratory Medicine of Shanghai Anticancer Association
  • Young Member of Immunology Technology Branch, Shanghai Society of Immunology
  • Member of Tumor Markers Professional Committee of Shanghai Anticancer Association
  • Member of the Oncology Working group of Shanghai Medical Doctor Association Laboratory Physician Society
  1. Sun X*, Tang F*, Guo Q*, Liu Y, He Y, Du Y, Gao F, Zhang G#, Yang C#. HAS2-Ezrin-ER axis plays a role in acquired antiestrogen resistance of ER-positive breast cancer. Front Pharmacol, 2022, doi: 10.3389/fphar.2022.1031487.  
  2. Gao F*#, Zhang G*, Liu Y, He Y, Sheng Y, Sun X, Du Y, Yang C#. Activation of CD44 signaling in leader cells induced by tumor-associated macrophages drives collective detachment in luminal breast carcinomas. Cell Death Dis, 2022, doi: 10.1038/s41419-022-04986-4. 
  3. Sheng Y*, Cao M*, Liu Y, He Y, Zhang G, Du Y, Gao F#, Yang C#. Hyaluronan synthase 2 (HAS2) regulates cell phenotype and invadopodia formation in luminal-like breast cancer cells. Mol Cell Biochem, 2021, doi: 10.1007/s11010-021-04165-7. 
  4. Zhang G*, He Y, Liu Y, Du Y, Yang C#, Gao F#. Reduced hyaluronan cross-linking induces breast cancer malignancy in a CAF-dependent manner. Cell Death Dis, 2021, doi: 10.1038/s41419-021-03875-6.       
  5. Hu S*, Shi X, Liu Y, He Y, Du Y, Zhang G, Yang C#, Gao F#. CD44 cross-linking increases malignancy of breast cancer via upregulation of p-Moesin. Cancer Cell Int, 2020, doi: 10.1186/s12935-020-01663-4.   
  6. Chen X*, Shi X*, Liu Y, He Y, Du Y, Zhang G, Yang C#, Gao F#. Remodelling of the bone marrow microenvironment by stromal hyaluronan modulates the malignancy of breast cancer cells. Cell Commun Signal, 2020, doi: 10.1186/s12964-020-00592-z.                  
  7. Yang C*, Sheng Y*, Shi X, Liu Y, He Y, Du Y, Zhang G, Gao F#. CD44/HA signaling mediates acquired resistance to a PI3Kα inhibitor. Cell Death Dis, 2020, doi: 10.1038/s41419-020-03037-0.  
  8. Yang C*, Cao M*, Liu Y, He Y, Du Y, Zhang G, Gao F#. Inducible formation of leader cells driven by CD44 switching gives rise to collective invasion and metastases in luminal breast carcinomas. Oncogene, 2019, doi: 10.1038/s41388-019-0899-y.       
  9. Yang C*, Liu Y, He Y, Du Y, Wang W, Shi X, Gao F#. The use of HA oligosaccharide-loaded nanoparticles to breach the endogenous hyaluronan glycocalyx for breast cancer therapy. Biomaterials, 2013, doi: 10.1016/j.biomaterials.2013.05.036. 
  10. Yang C*, Cao M*, Liu H, He Y, Xu J, Du Y, Liu Y, Wang W, Cui L, Hu J, Gao F#. The high and low molecular weight forms of hyaluronan have distinct effects on CD44 clustering. J Biol Chem, 2012, doi: 10.1074/jbc.M112.349209.   
  • 01/01/2023-12/31/2026
    National Natural Science Foundation of China (General Program), ¥520,000, 82273462
    The role and mechanism of "CD44-HA glycocalyx coat" on the surface of ER-positive breast cancer cells in endocrine therapy resistance
    Role: Project leader
  • 01/01/2020-12/31/2023
    National Natural Science Foundation of China (General Program), ¥550,000, 81974445
    Activation of CD44s/v switching in the leader cells of invading breast cancer cell clusters drives the shift from collective invasive to micro-mass shedding via a cross-talk with TAMs
    Role: Project leader
  • 01/01/2018-12/31/2020
    Shanghai Municipal Health Bureau, Municipal Medical and Health Development Foundation, ¥100,000, 2017
    Shanghai Outstanding Young Clinical Medical Talents (Clinical Laboratory)
    Role: Project leader
  • 07/01/2017-06/31/2020
    Shanghai Municipal Education Commission-Gaofeng Clinical Medicine Grant Support, ¥1,000,000, 20171924
    Inducible formation of leader cells driven by CD44/HA gives rise to collective invasion in breast cancer
    Role: Project leader 
  • 01/01/2017-12/31/2020
    National Natural Science Foundation of China (General Program), ¥540,000, 81672843
    The role and mechanism of HAS2 in regulating the abnormal accumulation of HA and promoting partial EMT and stemness acquisition in invasion and metastasis of breast cancer
    Role: Project leader  
  • 01/01/2015-12/31/2017
    National Natural Science Foundation of China (Younth Program), ¥230,000, 81402419
    The role and mechanism of HA/CD44 in the invasion of "leader cells" in breast cancer metastasis
    Role: Project leader                                                                                                                     
  • 07/01/2013-06/31/2014
    Shanghai Jiao Tong University School of Medicine Doctoral Innovation Fund, ¥30,000, BXJ201238
    Role of CD44 oligomerization mediated by HA in the formation of multidrug resistance in breast cancer
    Role: Project leader              
  • 10/01/2012-10/31/2015 
    Shanghai Natural Science Foundation (Younth Program), ¥100,000, 12ZR1447400
    The mechanism of drug resistance induced by HA-coat in breast cancer 
    Role: Project leader                                                                                                            
  1. [Feng Gao, Yiwen Liu, Yiqing He, Cuixia Yang, Hua Liu,] (2012), “Application and preparation of oHA-lipid-PTX nanoparticles for breast cancer therapy”; ZL 2012 1 0534240.0