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| 1 | Bone Morphogenetic Protein (BMP) signaling in development and human diseases显示文摘Bone Morphogenetic Proteins(BMPs)are a group of signaling molecules that belongs to the Transforming Growth Factor-b(TGF-b)superfamily of proteins.Initially discovered for their ability to induce bone formation,BMPs are now known to play crucial roles in all organ systems.BMPs are important in embryogenesis and development,and also in maintenance of adult tissue homeostasis.Mouse knockout models of various components of the BMP signaling pathway result in embryonic lethality or marked defects,highlighting the essential functions of BMPs.In this review,we first outline the basic aspects of BMP signaling and then focus on genetically manipulated mouse knockout models that have helped elucidate the role of BMPs in development.A significant portion of this review is devoted to the prominent human pathologies associated with dysregulated BMP signaling. | Richard N.Wang Jordan Green Zhongliang Wang Youlin Deng Min Qiao Michael Peabody Qian Zhang Jixing Ye Zhengjian Yan Sahitya Denduluri Olumuyiwa Idowu Melissa Li Christine Shen Alan Hu Rex C.Haydon Richard Kang James Mok Michael J.Lee Hue L.Luu Lewis L.Shi | 2014 | Genes & Diseases2014，1，1： | 47 |
| 2 | Insulin-like growth factor(IGF)signaling in tumorigenesis and the development of cancer drug resistance显示文摘One of the greatest obstacles to current cancer treatment efforts is the development of drug resistance by tumors.Despite recent advances in diagnostic practices and surgical interventions,many neoplasms demonstrate poor response to adjuvant or neoadjuvant radiation and chemotherapy.As a result,the prognosis for many patients afflicted with these aggressive cancers remains bleak.The insulin-like growth factor(IGF)signaling axis has been shown to play critical role in the development and progression of various tumors.Many basic science and translational studies have shown that IGF pathway modulators can have promising effects when used to treat various malignancies.There also exists a substantial body of recent evidence implicating IGF signaling dysregulation in the dwindling response of tumors to current standard-of-care therapy.By better understanding both the IGF-dependent and-independent mechanisms by which pathway members can influence drug sensitivity,we can eventually aim to use modulators of IGF signaling to augment the effects of current therapy.This review summarizes and synthesizes numerous recent investigations looking at the role of the IGF pathway in drug resistance.We offer a brief overview of IGF signaling and its general role in neoplasia,and then delve into detail about the many types of human cancer that have been shown to have IGF pathway involvement in resistance and/or sensitization to therapy.Ultimately,our hope is that such a compilation of evidence will compel investigators to carry out much needed studies looking at combination treatment with IGF signaling modulators to overcome current therapy resistance. | Sahitya K.Denduluri Olumuyiwa Idowu Zhongliang Wang Zhan Liao Zhengjian Yan Maryam K.Mohammed Jixing Ye Qiang Wei Jing Wang Lianggong Zhao Hue H.Luu | 2015 | Genes & Diseases2015，2，1： | 21 |
| 3 | Multifaceted signaling regulators of chondrogenesis:Implications in cartilage regeneration and tissue engineering显示文摘Defects of articular cartilage present a unique clinical challenge due to its poor self-healing capacity and avascular nature.Current surgical treatment options do not ensure consistent regeneration of hyaline cartilage in favor of fibrous tissue.Here,we review the current understanding of the most important biological regulators of chondrogenesis and their interactions,to provide insight into potential applications for cartilage tissue engineering.These include various signaling pathways,including fibroblast growth factors(FGFs),transforming growth factor b(TGF-b)/bone morphogenic proteins(BMPs),Wnt/b-catenin,Hedgehog,Notch,hypoxia,and angiogenic signaling pathways.Transcriptional and epigenetic regulation of chondrogenesis will also be discussed.Advances in our understanding of these signaling pathways have led to promising advances in cartilage regeneration and tissue engineering. | Jordan D.Green Viktor Tollemar Mark Dougherty Zhengjian Yan Liangjun Yin Jixing Ye Zachary Collier Maryam K.Mohammed Rex C.Haydon Hue H.Luu Richard Kang Michael J.Lee Sherwin H.Ho Tong-Chuan He Lewis L.Shi Aravind Athiviraham | 2015 | Genes & Diseases2015，2，4： | 9 |
| 4 | Wnt versus Hippo:A balanced act or dynamic duo?显示文摘The Hippo signaling pathway was first discovered in Drosophila as a conserved regulator of organ size.Genetic inactivation in mice demonstrates that the Hippo pathway functions as a fundamental inhibitor of organ growth during development,and as a critical tumor suppressor in epithelial tissues. | Zhongliang Wang Jixing Ye Youlin Deng Zhengjian Yan Sahitya Denduluri Tong-Chuan He | 2014 | Genes & Diseases2014，1，2： | 1 |
| 5 | Bone morphogenetic protein 2 inhibits the proliferation and growth ofhuman colorectal cancer cells显示文摘 | Yunyuan Zhang Xian Chen Min Qiao Bing-Qiang Zhang Ning Wang Zhonglin Zhang Zhan Liao Liyi Zeng Youlin Deng Fang Deng Junhui Zhang Liangjun Yin Wei Liu Qian Zhang Zhengjian Ya Jixing Ye Zhongliang Wang Lan Zhou Hue Luu Rex Haydon Tong-Chuan He Hongyu Zhang | 2014 | Oncology Reports2014，，3： | 1 |
| 6 | Pectin Methylesterases Enhance Root Cell Wall Phosphorus Remobilization in Rice显示文摘Pectin contributes greatly to cell wall phosphorus(P)remobilization.However,it is currently unclear whether the methylesterification degree of the pectin,which is related to the activity of pectin methylesterases(PMEs),is also involved in this process.Here,we demonstrated that elevated PME activity can facilitate the remobilization of P deposited in the cell wall.P-deficient conditions resulted in the reduction of root cell wall P content.This reduction was more pronounced in Nipponbare than in Kasalath,in company with a significant increment of the PME activity,indicating a possible relationship between elevated PME activity and cell wall P remobilization.This hypothesis was supported by in vitro experiments,as pectin with lower methylesterification degree had higher ability to release inorganic P(Pi)from insoluble FePO_(4).Furthermore,among the 35 OsPME members in rice,only the expression of OsPME14 showed a relationship with PME activity.In addition,transgenic rice lines overexpressing OsPME14 had increased PME activity,released more P from the root cell wall,and more resistant to P deficiency.In conclusion,PMEs enhance P remobilization in P-starved rice by increasing PME activity in Nipponbare,which in turn helps to remobilize P from the cell wall,and thus makes more available P. | WU Qi TAO Ye ZHANG Xiaolong DONG Xiaoying XIA Jixing SHEN Renfang ZHU Xiaofang | 2022 | Rice science2022，29，2： | 0 |
| 7 | Insider information:Testing cancer drug sensitivity for personalized therapy显示文摘Cancer death is usually caused by incurable drug-resistant and metastatic cancers.Although tremendous progress has been made in anticancer drug development during the past two decades,cancer medicine still faces unprecedented challenges associated with choosing effective treatments for individual patients.Three recent reports have offered encouraging approaches towards potentially personalized cancer drug selection. | Jing Wang Qiang Wei Jixing Ye Sahitya K.Denduluri Xin Wang Maryam K.Mohammed Hue H.Luu Rex C.Haydon Tong-Chuan He | 2015 | Genes & Diseases2015，2，3： | 0 |
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