Phenotypic heterogeneity of mycosis fungoides cells leads to the difficulties in determining tumour origin

IF 2.2 4区 医学 Q2 DERMATOLOGY Australasian Journal of Dermatology Pub Date : 2024-05-10 DOI:10.1111/ajd.14304
Sha Jin MMed, Yige Zhao MMed, Shiwen Wang MMed, Panpan Wang MMed, Chenyu Tang MMed, Mengyan Zhu MMed, Ping Wang PhD
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Abstract

Mycosis fungoides (MF) is a low-grade malignant cutaneous T-cell lymphoma that originates from memory T cells. It typically follows a unique and relatively indolent disease course. MF is used to be characterized by a tissue-resident memory T cell (TRM) phenotype, although recent molecular research has revealed its complexity, casting doubt on the cell of origin and the TRM-MF paradigm. Recent clonal heterogeneity studies suggest that MF may originate from immature early precursor T cells. During development, the tumour microenvironment (TME) influences tumour cell phenotype. The exact origin and development trajectory of MF remains elusive. Clarifying the origin of MF cells is vital for accurate diagnosis and effective treatment.

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真菌病细胞的表型异质性导致难以确定肿瘤来源。
放线菌病(MF)是一种起源于记忆 T 细胞的低度恶性皮肤 T 细胞淋巴瘤。它的病程通常比较特殊,病情相对较轻。MF过去以组织驻留记忆T细胞(TRM)表型为特征,但最近的分子研究揭示了它的复杂性,使人们对其起源细胞和TRM-MF范式产生了怀疑。最近的克隆异质性研究表明,MF 可能起源于未成熟的早期前体 T 细胞。在发育过程中,肿瘤微环境(TME)会影响肿瘤细胞的表型。中性粒细胞的确切起源和发育轨迹仍然难以捉摸。明确 MF 细胞的起源对于准确诊断和有效治疗至关重要。
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来源期刊
CiteScore
3.20
自引率
5.00%
发文量
186
审稿时长
6-12 weeks
期刊介绍: Australasian Journal of Dermatology is the official journal of the Australasian College of Dermatologists and the New Zealand Dermatological Society, publishing peer-reviewed, original research articles, reviews and case reports dealing with all aspects of clinical practice and research in dermatology. Clinical presentations, medical and physical therapies and investigations, including dermatopathology and mycology, are covered. Short articles may be published under the headings ‘Signs, Syndromes and Diagnoses’, ‘Dermatopathology Presentation’, ‘Vignettes in Contact Dermatology’, ‘Surgery Corner’ or ‘Letters to the Editor’.
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