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| 1 | Expression and thermostability of Paenibacillus campinasensis BL11 pectate lyase and its applications in bast fibre processing显示文摘 | C.‐H.Ko C.‐H.Tsai J.Tu S.‐H.Tang C.‐C.Liu | 2011 | Annals of Applied Biology2011，，2： | 1 |
| 2 | Brain magnetic resonance imaging abnormalities in neuromyelitis optica显示文摘 | Y.Li P.Xie F.Lv J.Mu Q.Li Q.Yang M.Hu H.Tang J.Yi | 2008 | Acta Neurologica Scandinavica2008，，4： | 1 |
| 3 | Capacity Reliability of a Road Network:An Assessment Methodology and Numerical Results显示文摘 | Anthony Chen Hai Yang Hong K.Lo Wilson H.Tang | | 0，，： | 1 |
| 4 | Astrometric observations of Nereid in 2006–2007显示文摘 | R. C.Qiao X.Cheng K. X.Shen G.Dourneau S. H.Wang X. Y.Hu Z. H.Tang X. J.Xi | 2008 | Monthly Notices of the Royal Astronomical Society2008，，4： | 1 |
| 5 | Neoadjuvant therapy of locally advanced gastric cancer显示文摘 | James J.Mezhir Laura H.Tang Daniel G.Coit | 2010 | J. Surg. Oncol2010，，4： | 1 |
| 6 | Desertification in north China: background, anthropogenic impacts and failures in combating it显示文摘 | Y.Chen H.Tang | 2005 | Land Degrad Dev2005，，4： | 1 |
| 7 | 查看详情显示文摘 | H.Tang F. Lévy H. Berger P.E.Schmid | | 0，，： | 1 |
| 8 | Neoadjuvant therapy of locally advanced gastric cancer显示文摘 | James J.Mezhir Laura H.Tang Daniel G.Coit | 2010 | J Surg Oncol2010，，4： | 1 |
| 9 | Persistent EGFR/K-RAS/SIAH pathway activation drives chemo-resistance and early tumor relapse in triple-negative breast cancer显示文摘Triple-negative breast cancer(TNBC)is the most aggressive breast cancer subtype.It disproportionately affects BRCA mutation carriers and young women,especially African American(AA)women.Chemoresistant TNBC is a heterogeneous and molecularly unstable disease that challenges our ability to apply personalized therapies.With the approval of immune checkpoint blockade(ICB)for TNBC,the addition of pembrolizumab to systemic chemotherapy has become standard of care(SOC)in neoadjuvant systemic therapy(NST)for high-risk early-stage TNBC.Pembrolizumab plus chemotherapy significantly increased the pathologic complete response(pCR)and improved event-free survival in TNBC.However,clinical uncertainties remain because similarly treated TNBC partial responders with comparable tumor responses to neoadjuvant therapy often experience disparate clinical outcomes.Current methods fall short in accurately predicting which high-risk patients will develop chemo-resistance and tumor relapse.Therefore,novel treatment strategies and innovative new research initiatives are needed.We propose that the EGFR-K-RAS-SIAH pathway activation is a major tumor driver in chemoresistant TNBC.Persistent high expression of SIAH in residual tumors following NACT/NST reflects that the EGFR/K-RAS pathway remains activated(ON),indicating an ineffective response to treatment.These chemoresistant tumor clones persist in expressing SIAH(SIAH^(High/ON))and are linked to early tumor relapse and poorer prognosis.Conversely,the loss of SIAH expression(SIAH^(Low/OFF))in residual tumors post-NACT/NST reflects EGFR/K-RAS pathway inactivation(OFF),indicating effective therapy and chemo-sensitive tumor cells.SIAH^(Low/OFF) signal is linked to tumor remission and better prognosis post-NACT/NST.Therefore,SIAH is well-positioned to become a novel tumor-specific,therapy-responsive,and prognostic biomarker.Potentially,this new biomarker(SIAH^(High/ON))could be used to quantify therapy response,predict chemo-resistance,and identify those patients at the highest risk for tumor relapse and poor survival in TNBC. | Amy H.Tang Richard A.Hoefer Mary L.Guye Harry D.Bear | 2022 | Cancer Drug Resistance2022，5，3： | 1 |
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