不适合移植的大 B 细胞淋巴瘤二线使用 axicabtagene ciloleucel:ALYCANTE 最终分析
Second-line axicabtagene ciloleucel in large B-cell lymphoma ineligible for transplantation: ALYCANTE final analysis.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Transcriptomic and differential gene analysis investigating the differences in biological behaviour between subtypes of feline alimentary lymphoma.
Transcriptomic and differential gene analysis investigating the differences in biological behaviour between subtypes of feline alimentary lymphoma.
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猫消化道淋巴瘤包括多种肿瘤亚型,这些亚型可能源自不同细胞群,在生物学行为和预后方面差异显著。新一代测序技术已日益用于人类淋巴瘤的诊断、预后判断和治疗,但在猫消化道淋巴瘤研究中的应用仍较少。目前该领域研究主要集中于区分惰性肠道淋巴瘤与炎症性肠病。
本研究旨在通过转录组分析识别差异表达基因,探索其与不同亚型猫消化道淋巴瘤侵袭性的关联。研究对19例猫消化道淋巴瘤的RNA测序数据进行差异基因分析;依据组织形态学和免疫组化将其分为五种表型:小T细胞型、B细胞型、CD56⁺ B细胞型、大颗粒T细胞型和大颗粒NK细胞型。侵袭性淋巴瘤类型中过表达的基因包括多种参与细胞外基质重塑、转录因子表达、细胞分裂、信号传导及代谢的基因(ADAMTS14、ADAMTS12、FOXI3、ELAVL2、CCR1、GCGR、NMUR1、MARC1、SLC29A4、CENPF、IGF2BP3);惰性淋巴瘤类型中过表达的则包括若干肿瘤抑制基因(RAB17、SYNPO2、GRM4)。这些差异表达与生物学行为相关。未来利用分子、免疫组化或原位杂交技术进一步研究这些基因或其产物的表达,或可显著改善猫消化道淋巴瘤预后判断,并为开发针对特定亚型的靶向免疫治疗铺路。
Feline alimentary lymphoma encompasses a diverse group of neoplastic subtypes, each presumably arising from distinct cell populations and exhibiting significant variability in biological behaviour and prognosis. Whilst next-generation sequencing technologies have become a more common aid in the diagnosis, prognostication and treatment of lymphoma in humans, these techniques have been sparsely applied to investigate feline alimentary lymphoma. Specifically, current research in this field is mostly focused on differentiating indolent intestinal lymphomas from inflammatory enteropathies. The aim of the study was to apply transcriptomic analysis to identify differentially expressed genes that may correlate with the aggressiveness of various subtypes of feline alimentary lymphoma. Differential gene analysis was applied to RNA sequencing data from 19 cases of feline alimentary lymphoma split into five phenotypes (small T cell, B cell, CD56+ B cell, Large Granular T cell and Large Granular NK cell lymphomas) according to histomorphology and immunohistochemistry.
The analysis identified overexpression of several genes involved in extracellular matrix remodelling, transcription factor expression and cellular division, signalling and metabolism in aggressive lymphoma types (ADAMTS14, ADAMTSl2, FOXI3, ELAVL2, CCR1, GCGR, NMUR1, MARC1, SLC29A4, CENPF, IGF2BP3); and overexpression of several tumour suppressor genes in the indolent lymphoma type (RAB17, SYNPO2, GRM4).
The differential expression correlated with biologic behaviours. Future investigation into expression of these genes or gene products using molecular, immunohistochemical or in-situ hybridisation techniques could yield significant advancements in the prognostication of feline alimentary lymphoma as well as pave the way for the development of targeted immunotherapeutic strategies to aid in the treatment of specific feline alimentary lymphoma subtypes.
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