Liu Xibo, Xu Jinghong, Chen Lirong
Department of Pathology, The Second Affiliated Hospital Zhejiang University School of Medicine, Hangzhou 310009, China.
Oncotarget. 2017 Jun 20;8(39):65407-65413. doi: 10.18632/oncotarget.18577. eCollection 2017 Sep 12.
Osseous metaplasia (OM) is rarely observed in colorectal cancer (incidence < 0.4% in rectal cancer), where it has a non-specific clinical presentation and unknown pathogenesis. Here, we report three cases of colorectal carcinoma with OM and propose a new hypothesis. All three patients (two males and one female) were Chinese and had different sites of colorectal carcinoma with OM: rectum, sigmoid colon, and appendix. The pathologic diagnoses were serrated adenocarcinoma; moderately to poorly differentiated adenocarcinoma with micropapillary carcinoma and cribriform comedo-type adenocarcinoma; and mucinous adenocarcinoma, respectively. Clinical follow-up showed that one patient died 5 months after surgery, but the others are alive after 68 months and 53 months. Immunohistochemistry revealed that CD44, MAPK, MDM2, OPN and PEDF were expressed by both tumor cells and stromal cells, while P53 was expressed only by tumor cells. KRAS/NRAS/BRAF genotyping revealed different KRAS mutations in each of the three cases, but the NRAS and BRAF exons were all wild-type. These findings suggest OM has no relation with NRAS and BRAF mutation, and it is uncertain whether there is a relationship between ossification and KRAS mutation. OPN, MAPK, MDM2, P53, PEDF and CD44 may act as osteogenic factors in colorectal cancer with OM.
骨化生(OM)在结直肠癌中很少见(直肠癌发病率<0.4%),其临床表现不特异,发病机制不明。在此,我们报告3例伴有OM的结直肠癌病例并提出一个新假说。所有3例患者(2例男性,1例女性)均为中国人,结直肠癌伴OM的部位不同:直肠、乙状结肠和阑尾。病理诊断分别为锯齿状腺癌;伴微乳头癌和筛状粉刺型腺癌的中分化至低分化腺癌;黏液腺癌。临床随访显示,1例患者术后5个月死亡,但其他患者分别在68个月和53个月后仍存活。免疫组化显示,肿瘤细胞和基质细胞均表达CD44、MAPK、MDM2、OPN和PEDF,而P53仅由肿瘤细胞表达。KRAS/NRAS/BRAF基因分型显示3例患者均有不同的KRAS突变,但NRAS和BRAF外显子均为野生型。这些发现提示OM与NRAS和BRAF突变无关,骨化与KRAS突变之间是否存在关联尚不确定。OPN、MAPK、MDM2、P53、PEDF和CD44可能在伴有OM的结直肠癌中作为成骨因子起作用。