Fukushima Noriyasu, Satoh Toshimi, Sueoka Naoko, Sato Akemi, Ide Masaru, Hisatomi Takashi, Kuwahara Nobuo, Tomimasu Rika, Tsuneyoshi Naoko, Funai Noriko, Sano Masayuki, Tokunaga Osamu, Sueoka Eisaburo
Department of Internal Medicine, Faculty of Medicine, Saga University, Saga-City, Saga, Japan.
Cancer Sci. 2006 Oct;97(10):1050-5. doi: 10.1111/j.1349-7006.2006.00284.x. Epub 2006 Aug 17.
A member of the family of p53-related genes, p63 plays a role in regulating epithelial proliferation and differentiation programs, but the pathological and clinical meaning of p63 in B-cell lymphoma has not been elucidated. We investigated the expression pattern of p63 in B-cell malignancies, and evaluated the correlation between the expression of p63 and other germinal center markers. Ninety-eight B-cell lymphomas (28 FCL, 5 MCL, and 65 DLBCL) were analyzed by immunohistochemical examination for p63, bcl-6, CD10 and MUM-1 proteins, and for rearrangement of bcl-2/IgH. Expression of p63 was observed in the nuclei of tumor cells obtained from 15 of 28 (54%) FCL, 22 of 65 (34%) DLBCL, but none of 5 MCL. In DLBCL, the expression of p63 and bcl-6 showed a significant correlation (P < 0.02), but no correlation was observed between p63 and expression of CD10, MUM-1, or bcl-2/IgH rearrangement. RT-PCR revealed that TAp63alpha-type transcripts, a possible negative regulator of transcriptional activation of p21 promoter, were major transcripts in B-cell lymphoma tissues. As for prognostic significance, only patients in the p63 positive group of FCL died, and in the non-germinal center group, the p63 positive cases appeared to have inferior overall survival than other groups in DLBCL. Our preliminary results suggested that p63 expression is a disadvantageous factor for prognosis in this subgroup of B-cell lymphomas.
p63是p53相关基因家族的成员之一,在调节上皮细胞增殖和分化程序中发挥作用,但p63在B细胞淋巴瘤中的病理和临床意义尚未阐明。我们研究了p63在B细胞恶性肿瘤中的表达模式,并评估了p63表达与其他生发中心标志物之间的相关性。通过免疫组织化学检查分析了98例B细胞淋巴瘤(28例滤泡性淋巴瘤、5例套细胞淋巴瘤和65例弥漫性大B细胞淋巴瘤)中的p63、bcl-6、CD10和MUM-1蛋白表达情况以及bcl-2/IgH重排情况。在28例滤泡性淋巴瘤中的15例(54%)、65例弥漫性大B细胞淋巴瘤中的22例(34%)的肿瘤细胞核中观察到p63表达,但5例套细胞淋巴瘤中均未观察到。在弥漫性大B细胞淋巴瘤中,p63和bcl-6的表达呈显著相关(P < 0.02),但p63与CD10、MUM-1的表达或bcl-2/IgH重排之间未观察到相关性。逆转录聚合酶链反应显示,TAp63α型转录本是B细胞淋巴瘤组织中的主要转录本,TAp63α型转录本可能是p21启动子转录激活的负调节因子。至于预后意义,仅滤泡性淋巴瘤p63阳性组的患者死亡,在非生发中心组中,弥漫性大B细胞淋巴瘤p63阳性病例的总生存期似乎比其他组差。我们的初步结果表明,p63表达是该亚组B细胞淋巴瘤预后的不利因素。