维普中文期刊产品整合服务
13篇 您的检索式:作者名="Jacintha"
    题名 作者 年代 出处 被引量
1Leukemic stromal hematopoietic microenvironment negatively regulates the normal hematopoiesis in mouse model of leukemia显示文摘Background and Objective: Leukemic microenvironment has a major role in the progression of leukemia. Leukemic cells can induce reversible changes in microenvironmental components, especially the stromal function which results in improved growth conditions for maintaining the malignant leukemic cells. This study aimed to investigate the survival advantage of leukemic cells over normal hematopoietic cells in stromal microenvironment in long term. Methods: The mice were injected intraperitoneally with N-N’ ethylnitrosourea (ENU) to induce leukemia; the mice received injection of normal saline were used as control. At 180 days after ENU induction, the mice were killed and the bone marrows were cultured for 19 days. Colony-forming assays were used to analyze the formation of various cell colonies. The expression of Sca-1, CD146, VEGFR2, CD95, pStat3, pStat5, and Bcl-xL in marrow cells were detected by flow cytometry. Results: Long-term leukemic bone marrow culture showed abnormal elongated stromal fibroblasts with almost absence of normal hematopoietic cells. Adherent cell colonies were increased, but CFU-F and other hematopoietic cell colonies were significantly decreased in leukemia group (P< 0.001). Primitive progenitor-specific Sca-1 receptor expression was decreased with subsequent increased expression of CD146 and VEGFR-2 in leukemic bone marrow cells. Decreased Fas antigen expression with increased intracellular pStat3, pStat5 and Bcl-xL proteins were observed in leukemic bone marrow cells. Conclusions: Stromal microenvironment shows altered morphology and decreased maturation in leukemia. Effective progenitor cells are decreased in leukemia with increased leukemia-specific cell population. Leukemic microenvironment plays a role in promoting and maintaining the leukemic cell proliferation and survivability in long term.Pratima Basak Sumanta Chatterjee Prosun Das Madhurima Das Jacintha Archana Pereira Ranjan Kumar Dutta Malay Chaklader Samaresh Chaudhuri Sujata Law 2010Chinese Journal of Cancer2010,29,12:3
2The effect of different dietary sugars and honey on longevity and fecundity in two hyperparasitoid wasps显示文摘Jeffrey A. Harvey Josianne Cloutier Bertanne Visser Jacintha Ellers Felix L. W?ckers Rieta Gols 2012Journal of Insect Physiology2012,,6:1
3Lack of lipogenesis in parasitoids: A review of physiological mechanisms and evolutionary implications显示文摘Bertanne Visser Jacintha Ellers 2008Journal of Insect Physiology2008,,9:1
4Wolbachia endosymbiont is essential for egg hatching in a parthenogenetic arthropod显示文摘Martijn J. T. N. Timmermans Jacintha Ellers 2009Evolutionary Ecology2009,,6:1
5Could Signal Transducer and Activator of Transcription 3 be a Therapeutic Target in Obesity-Related Gastrointestinal Malignancy?显示文摘Katie E. O’Sullivan John V. Reynolds Ciara O’Hanlon Jacintha N. O’Sullivan Joanne Lysaght 2014Journal of Gastrointestinal Cancer2014,,1:1
6Determinants of short- and long-term survival from colorectal cancer in very elderly patients显示文摘Juliette Sheridan Paul Walsh David Kevans Therese Cooney Shane O’Hanlon Blathnaid Nolan Anne White Edel McDermott Kieran Sheahan Diarmuid O’Shea John Hyland Diarmuid O’Donoghue Jacintha O’Sullivan Hugh Mulcahy Glen Doherty 2014Journal of Geriatric Oncology2014,,:1
7Persistent net bone formation at one year due to local elution of zoledronic acid from porous tantalum implants显示文摘Michael T Dorota K Jacintha R 0,,:1
8Stage II colonic adenocarcinoma: a detailed study of pT4N0 with emphasis on peritoneal involvement and the role of tumour budding显示文摘Aoife L Canney David Kevans Lai Mun Wang John M P Hyland Hugh E Mulcahy Diarmuid P O’Donoghue Jacintha O’Sullivan Robert Geraghty Kieran Sheahan 2012Histopathology2012,,3:1
9Histopathologic retrieval analysis of clinically failed porous tantalum osteonecrosis implants显示文摘Michael T Dorota K Jacintha R 0,,:1
10Impact of radiotherapy on the immune landscape in oesophageal adenocarcinoma显示文摘BACKGROUND In the contemporary era of cancer immunotherapy,an abundance of clinical and translational studies have reported radiotherapy(RT)and immunotherapies as a viable option for immunomodulation of many cancer subtypes,with many related clinical trials ongoing.In locally advanced disease,chemotherapy or chemoradiotherapy followed by surgical excision of the tumour remain the principal treatment strategy in oesophageal adenocarcinoma(OAC),however,the use of the host immune system to improve anti-tumour immunity is rapidly garnering increased support in the curative setting.AIM To immunophenotype OAC patients’immune checkpoint(IC)expression with and without radiation and evaluate the effects of checkpoint blockade on cell viability.METHODS In the contemporary era of cancer immunotherapy,an abundance of studies have demonstrated that combination RT and IC inhibitors(ICIs)are effective in the immunomodulation of many cancer subtypes,with many related clinical trials ongoing.Although surgical excision and elimination of tumour cells by chemotherapy or chemoradiotherapy remains the gold standard approach in OAC,the propagation of anti-tumour immune responses is rapidly garnering increased support in the curative setting.The aim of this body of work was to immunophenotype OAC patients’IC expression with and without radiation and to establish the impact of checkpoint blockade on cell viability.This study was a hybrid combination of in vitro and ex vivo models.Quantification of serum immune proteins was performed by enzyme-linked immunosorbent assay.Flow cytometry staining was performed to evaluate IC expression for in vitro OAC cell lines and ex vivo OAC biopsies.Cell viability in the presence of radiation with and without IC blockade was assessed by a cell counting kit-8 assay.RESULTS We identified that conventional dosing and hypofractionated approaches resulted in increased IC expression(PD-1,PD-L1,TIM3,TIGIT)in vitro and ex vivo in OAC.There were two distinct subcohorts with one demonstrating significant upregulation of ICs and the contrary in the other cohort.Increasing IC expression post RT was associated with a more aggressive tumour phenotype and adverse features of tumour biology.The use of anti-PD-1 and anti-PD-L1 immunotherapies in combination with radiation resulted in a significant and synergistic reduction in viability of both radiosensitive and radioresistant OAC cells in vitro.Interleukin-21(IL-21)and IL-31 significantly increased,with a concomitant reduction in IL-23 as a consequence of 4 Gray radiation.Similarly,radiation induced an anti-angiogenic tumour milieu with reduced expression of vascular endothelial growth factor-A,basic fibroblast growth factor,Flt-1 and placental growth factor.CONCLUSION The findings of the current study demonstrate synergistic potential for the use of ICIs and ionising radiation to potentiate established anti-tumour responses in the neoadjuvant setting and is of particular interest in those with advanced disease,adverse features of tumour biology and poor treatment responses to conventional therapies.Noel E Donlon Maria Davern Fiona O'Connell Andrew Sheppard Aisling Heeran Anshul Bhardwaj Christine Butler Ravi Narayanasamy Claire Donohoe James J Phelan Niamh Lynam-Lennon Margaret R Dunne Stephen Maher Jacintha O'Sullivan John V Reynolds Joanne Lysaght 2022World Journal of Gastroenterology2022,28,21:1
11γ–aminobutyric acid promotes stem elongation in Stellaria longipes: The role of ethylene显示文摘Arumugam Kathiresan Jacintha Miranda C.C. Chinnappa D.M. Reid 1998Plant Growth Regulation1998,,2:1
12Taxol Content of Irish Yews显示文摘Jacintha Gruffin Ingrid Hook 1996Planta Med1996,,62:1
13Modeling and stability analysis of the spread of novel coronavirus disease COVTD-19显示文摘Towards the end of 2019,the world witnessed the outbreak of Severe Acute Respiratory Syndrome Coronavirus-2(COVID-19),a new strain of coronavirus that was unidentified in humans previously.In this paper,a new fractional-order Susceptible-Exposed-Infected-Hospitalized-Recovered(SEIHR)model is formulated for COVID-19,where the population is infected due to human transmission.The fractional-order discrete version of the model is obtained by the process of discretization and the basic reproductive number is calculated with the next-generation matrix approach.All equilibrium points related to the disease transmission model are then computed.Further,sufficient conditions to investigate all possible equilibria of the model are established in terms of the basic reproduction number(local stability)and are supported with time series,phase portraits and bifurcation diagrams.Finally,numerical simulations are provided to demonstrate the theoretical findings.A.George Maria Selvam Jehad Alzabut D.Abraham Vianny Mary Jacintha Fatma Bozkurt Yousef 2021International Journal of Biomathematics2021,14,5:0
返回顶部 每页显示:
共1页 首页 上一页 第1页 下一页 末页 /1 跳转

网站首页 | 关于我们 | 联系我们 | 产品服务 | 客服中心 | 广告服务 | 版权声明 | 网站联盟 | 友情链接 | 售卡网点

版权所有© 渝B2-20050021-1 渝公网安备 50019002500403号 违法和不良信息举报中心

互联网出版许可证 新出网证(渝)字10号 全国400电话 - 免长途话费