Serum insulin‐like growth factor binding protein 2 levels as biomarker for pancreatic ductal adenocarcinoma‐associated malnutrition and muscle wasting
暂无分享,去创建一个
Hongwei Wang | Song Gao | Zekun Li | Shengyu Yang | Jie Yu | Liangliang Wu | T. Zhao | Xiuchao Wang | J. Hao | C. Lan | Jie Dong | Chun-tao Gao | Zhe Liu | Chungen Lan | Tiansuo Zhao | Jie Dong
[1] Yueying Li,et al. Serum IGFBP2 Level Is a New Candidate Biomarker of Severe Malnutrition in Advanced Lung Cancer , 2020, Nutrition and cancer.
[2] M. Karamouzis,et al. Pancreatic Cancer and Cachexia—Metabolic Mechanisms and Novel Insights , 2020, Nutrients.
[3] Swarnali Acharyya,et al. Understanding cachexia in the context of metastatic progression , 2020, Nature Reviews Cancer.
[4] R. Medeiros,et al. Cancer cachexia and its pathophysiology: links with sarcopenia, anorexia and asthenia , 2020, Journal of cachexia, sarcopenia and muscle.
[5] G. Fuller,et al. IGFBP2: integrative hub of developmental and oncogenic signaling network , 2020, Oncogene.
[6] Guohao Wu,et al. Sarcopenia as a predictor of poor surgical and oncologic outcomes after abdominal surgery for digestive tract cancer: A prospective cohort study. , 2019, Clinical nutrition.
[7] J. Prados,et al. The challenge of drug resistance in pancreatic ductal adenocarcinoma: a current overview , 2019, Cancer biology & medicine.
[8] J. Trevino,et al. Molecular therapeutic strategies targeting pancreatic cancer induced cachexia , 2018, World journal of gastrointestinal surgery.
[9] S. Herzig,et al. Cancer Cachexia: More Than Skeletal Muscle Wasting. , 2018, Trends in cancer.
[10] S. Theocharis,et al. Clinical Value of Nutritional Status in Cancer: What is its Impact and how it Affects Disease Progression and Prognosis? , 2017, Nutrition and cancer.
[11] F. Ottery,et al. Assessing nutritional status in cancer: role of the Patient-Generated Subjective Global Assessment , 2017, Current opinion in clinical nutrition and metabolic care.
[12] Wei Zhang,et al. IGFBP2 Activates the NF-κB Pathway to Drive Epithelial-Mesenchymal Transition and Invasive Character in Pancreatic Ductal Adenocarcinoma. , 2016, Cancer research.
[13] Zhou Yuan,et al. Pancreatic cancer cell-derived IGFBP-3 contributes to muscle wasting , 2016, Journal of Experimental & Clinical Cancer Research.
[14] L. Jia,et al. Single nucleotide polymorphism in the microRNA-199a binding site of HIF1A gene is associated with pancreatic ductal adenocarcinoma risk and worse clinical outcomes , 2016, Oncotarget.
[15] Lun Zhang,et al. IGF-binding protein 2 is a candidate target of therapeutic potential in cancer , 2016, Tumor Biology.
[16] Y. Bang,et al. Skeletal Muscle Depletion Predicts the Prognosis of Patients with Advanced Pancreatic Cancer Undergoing Palliative Chemotherapy, Independent of Body Mass Index , 2015, PloS one.
[17] G. Mantovani,et al. Muscle wasting as main evidence of energy impairment in cancer cachexia: future therapeutic approaches. , 2015, Future oncology.
[18] N. Perrimon,et al. Systemic organ wasting induced by localized expression of the secreted insulin/IGF antagonist ImpL2. , 2015, Developmental cell.
[19] D. McCance,et al. IGF-Binding Protein 2 – Oncogene or Tumor Suppressor? , 2015, Front. Endocrinol..
[20] Yan Sun,et al. Stem cell factor is a novel independent prognostic biomarker for hepatocellular carcinoma after curative resection. , 2014, Carcinogenesis.
[21] M. Martignoni,et al. Cachexia and pancreatic cancer: are there treatment options? , 2014, World journal of gastroenterology.
[22] K. Boucher,et al. Serum IGFBP2 and MSLN as diagnostic and prognostic biomarkers for pancreatic cancer. , 2014, HPB : the official journal of the International Hepato Pancreato Biliary Association.
[23] S. Lo,et al. Pancreatic cancer cachexia: a review of mechanisms and therapeutics , 2014, Front. Physiol..
[24] N. Perrimon,et al. Mechanisms of muscle growth and atrophy in mammals and Drosophila , 2014, Developmental dynamics : an official publication of the American Association of Anatomists.
[25] Xifeng Wu,et al. Insulin-Like Growth Factor Binding Protein-2 Level Is Increased in Blood of Lung Cancer Patients and Associated with Poor Survival , 2013, PloS one.
[26] L. Mccargar,et al. Cancer cachexia in the age of obesity: skeletal muscle depletion is a powerful prognostic factor, independent of body mass index. , 2013, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[27] Yun-Ru Chen,et al. Development of IGF Signaling Antibody Arrays for the Identification of Hepatocellular Carcinoma Biomarkers , 2012, PloS one.
[28] J. Sabate,et al. Malnutrition Is High and Underestimated During Chemotherapy in Gastrointestinal Cancer: An AGEO Prospective Cross-Sectional Multicenter Study , 2012, Nutrition and cancer.
[29] C. Bloomfield,et al. High expression of IGFBP2 is associated with chemoresistance in adult acute myeloid leukemia. , 2011, Leukemia research.
[30] Paula Ravasco,et al. Definition and classification of cancer cachexia: an international consensus. , 2011, The Lancet. Oncology.
[31] D. Cella,et al. Muscle wasting in cancer cachexia: clinical implications, diagnosis, and emerging treatment strategies. , 2011, Annual review of medicine.
[32] Hsiu‐Po Wang,et al. Plasma insulin-like growth factor-binding protein-2 levels as diagnostic and prognostic biomarker of colorectal cancer. , 2010, The Journal of clinical endocrinology and metabolism.
[33] Y. Ishikawa,et al. Role of insulin-like growth factor binding protein 2 in lung adenocarcinoma: IGF-independent antiapoptotic effect via caspase-3. , 2010, The American journal of pathology.
[34] Wei Zhang,et al. Plasma IGFBP-2 levels predict clinical outcomes of patients with high-grade gliomas. , 2009, Neuro-oncology.
[35] Tony Reiman,et al. Prevalence and clinical implications of sarcopenic obesity in patients with solid tumours of the respiratory and gastrointestinal tracts: a population-based study. , 2008, The Lancet. Oncology.
[36] P. Marques‐Vidal,et al. Serum concentrations of TNF-alpha as a surrogate marker for malnutrition and worse quality of life in patients with gastric cancer. , 2007, Clinical nutrition.
[37] M. Stampfer,et al. Circulating insulin-like growth factor axis and the risk of pancreatic cancer in four prospective cohorts , 2007, British Journal of Cancer.
[38] Xiao-qun Zhu,et al. Expression of insulin-like growth factor binding protein-2 in gastric carcinoma and its relationship with cell proliferation. , 2006, World journal of gastroenterology.
[39] Stanley Heshka,et al. Total body skeletal muscle and adipose tissue volumes: estimation from a single abdominal cross-sectional image. , 2004, Journal of applied physiology.
[40] R. Baxter,et al. Cellular actions of the insulin-like growth factor binding proteins. , 2002, Endocrine reviews.
[41] A. Inui. Cancer Anorexia‐Cachexia Syndrome: Current Issues in Research and Management , 2002, CA: a cancer journal for clinicians.
[42] M. Kattan,et al. Association of preoperative plasma levels of insulin-like growth factor I and insulin-like growth factor binding proteins-2 and -3 with prostate cancer invasion, progression, and metastasis. , 2002, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[43] D J Glass,et al. Identification of Ubiquitin Ligases Required for Skeletal Muscle Atrophy , 2001, Science.
[44] T. Rohan,et al. Role of the insulin-like growth factor family in cancer development and progression. , 2000, Journal of the National Cancer Institute.
[45] E. Diamandis,et al. Pancreatic cancer. , 2013, Clinical chemistry.
[46] Hang-bo Zhou,et al. Expression of IGFBP2 in Gastric Carcinoma and Relationship With Clinicopathologic Parameters and Cell Proliferation , 2006, Digestive Diseases and Sciences.
[47] C. Potten,et al. The Journal of Clinical Endocrinology & Metabolism Printed in U.S.A. Copyright © 2000 by The Endocrine Society Circulating Insulin-Like Growth Factor II and , 2000 .
[48] Stampfer,et al. Prospective study of colorectal cancer risk in men and plasma levels of insulin-like growth factor (IGF)-I and IGF-binding protein-3. , 1999, Journal of the National Cancer Institute.