Tagami Mizuki, Isayama Keishiro, Nishio Mizuho, Yoshikawa Atsuko, Misawa Norihiko, Sakai Atsushi, Haruna Yusuke, Tomita Mami, Mizukami Yoichi, Azumi Atsushi, Honda Shigeru
Department of Ophthalmology and Visual Sciences, Graduate School of Medicine, Osaka Metropolitan University, 1-5-7 Asahimachi, Abeno-ku, Osaka-shi, 545-8586, Osaka, Japan.
Ophthalmology Department and Eye Center, Kobe Kaisei Hospital, Kobe, Hyogo, Japan.
Discov Oncol. 2025 Aug 4;16(1):1466. doi: 10.1007/s12672-025-03239-y.
Mucosa-associated lymphoid tissue (MALT) lymphoma in the orbital region and IgG4-related ophthalmic disease (IgG4-ROD) account for the majority of mass lesions in the orbital region. These diseases may show similar shadows on radiologic images, and many cases are difficult to differentiate clinically. Using histology, we investigated the gene expression clusters (RNA-seq) and molecular differences responsible for these two diseases.
Retrospective cohort study.
Patients diagnosed with orbital MALT and IgG4-ROD who underwent surgical treatment at Osaka Metropolitan University or Kobe Kaisei Hospital, Japan, were included in the study.
Fresh tissues extracted from 20 cases of MALT lymphoma and IgG4-ROD histopathologically diagnosed were subjected to next-generation sequencing analysis, and a sequence library was generated. Next-generation sequencing analysis was performed to compare gene expression between the two groups, and principal component and cluster hierarchy analyses were performed. Genes exhibiting significant changes in expression were examined individually after pathway analysis; immunohistochemical staining was performed to determine the intensity and staining morphology of components of significantly altered pathways.
Gene cluster differences between orbital MALT lymphoma and IgG4-ROD.
In principal component analysis, orbital MALT lymphoma and IgG4-ROD clustered in component 2. Clear cluster differences were observed, except for one case that appeared to be IgG4-producing MALT lymphoma. This apparent case of IgG4-producing MALT lymphoma clustered just between the IgG4-ROD and MALT lymphoma clusters. Analysis of upregulated genes between IgG4-ROD and MALT lymphoma identified 582 candidate genes (P < 0.01). Pathway analysis of MALT lymphoma suggested that the STING pathway was activated. Downstream pathway analysis identified eight significant gene expression changes (P < 0.05). STING immunohistochemical analysis indicated a quantitative difference in staining pattern between IgG4-ROD and MALT lymphoma (P < 0.01). STING-positive staining within cells was significantly greater in MALT than the Golgi complex near the nucleus.
Orbital MALT lymphoma and IgG4-ROD can be differentiated by two gene expression clusters. The STING pathway may play a more important role in orbital MALT lymphoma than orbital IgG4-ROD.
眼眶区域的黏膜相关淋巴组织(MALT)淋巴瘤和IgG4相关性眼病(IgG4-ROD)占眼眶区域大多数肿块病变。这些疾病在放射影像上可能显示相似的阴影,并且许多病例在临床上难以鉴别。我们利用组织学研究了这两种疾病的基因表达簇(RNA测序)和分子差异。
回顾性队列研究。
纳入在日本大阪市立大学或神户开成医院接受手术治疗的诊断为眼眶MALT淋巴瘤和IgG4-ROD的患者。
对20例经组织病理学诊断的MALT淋巴瘤和IgG4-ROD患者提取的新鲜组织进行二代测序分析,并构建序列文库。进行二代测序分析以比较两组之间的基因表达,并进行主成分分析和聚类层次分析。在通路分析后单独检查表达有显著变化的基因;进行免疫组织化学染色以确定显著改变通路的成分的强度和染色形态。
眼眶MALT淋巴瘤和IgG4-ROD之间的基因簇差异。
在主成分分析中,眼眶MALT淋巴瘤和IgG4-ROD聚集在成分2中。观察到明显的簇差异,除了1例似乎是产生IgG4的MALT淋巴瘤。这例明显的产生IgG4的MALT淋巴瘤正好聚集在IgG4-ROD和MALT淋巴瘤簇之间。对IgG4-ROD和MALT淋巴瘤之间上调基因的分析确定了582个候选基因(P<0.01)。MALT淋巴瘤的通路分析表明STING通路被激活。下游通路分析确定了8个显著的基因表达变化(P<0.05)。STING免疫组织化学分析表明IgG4-ROD和MALT淋巴瘤在染色模式上存在定量差异(P<0.01)。MALT中细胞内STING阳性染色明显大于细胞核附近的高尔基体。
眼眶MALT淋巴瘤和IgG4-ROD可通过两个基因表达簇进行鉴别。STING通路在眼眶MALT淋巴瘤中可能比眼眶IgG4-ROD发挥更重要的作用。