Yang Ye, Wen Wu, Chen Feng-Lin, Zhang Ying-Jie, Liu Xiao-Cong, Yang Xiao-Yan, Hu Shan-Shan, Jiang Ye, Yuan Jing
Digestive Diseases, Chengdu Qingbaijiang District People's Hospital, Chengdu 610300, Sichuan Province, China.
Digestive Diseases, Chengdu Second People's Hospital, Chengdu 610000, Sichuan Province, China.
World J Gastrointest Oncol. 2024 Mar 15;16(3):670-686. doi: 10.4251/wjgo.v16.i3.670.
The incidence and mortality of colorectal cancer (CRC) are among the highest in the world, and its occurrence and development are closely related to tumor neovascularization. When the balance between pigment epithelium-derived factors (PEDF) that inhibit angiogenesis and vascular endothelial growth factors (VEGF) that stimulate angiogenesis is broken, angiogenesis is out of control, resulting in tumor development. Therefore, it is very necessary to find more therapeutic targets for CRC for early intervention and later treatment.
To investigate the expression and significance of PEDF, VEGF, and CD31-stained microvessel density values (CD31-MVD) in normal colorectal mucosa, adenoma, and CRC.
In this case-control study, we collected archived wax blocks of specimens from the Digestive Endoscopy Center and the General Surgery Department of Chengdu Second People's Hospital from April 2022 to October 2022. Fifty cases of specimen wax blocks were selected as normal intestinal mucosa confirmed by electronic colonoscopy and concurrent biopsy (normal control group), 50 cases of specimen wax blocks were selected as colorectal adenoma confirmed by electronic colonoscopy and pathological biopsy (adenoma group), and 50 cases of specimen wax blocks were selected as CRC confirmed by postoperative pathological biopsy after inpatient operation of general surgery (CRC group). An immunohistochemical staining experiment was carried out to detect PEDF and VEGF expression in three groups of specimens, analyze their differences, study the relationship between the two and clinicopathological factors in CRC group, record CD31-MVD in the three groups, and analyze the correlation of PEDF, VEGF, and CD31-MVD in the colorectal adenoma group and the CRC group. The test or adjusted test is used to analyze measurement data statistically. Kruskal-Wallis rank sum test was used between groups for ranked data. The chi-square test, adjusted chi-square test, or Fisher's exact test were used to compare the rates between groups. All differences between groups were compared using the Bonferroni method for multiple comparisons. Spearman correlation analysis was used to test the correlation of the data. The test level () was 0.05, and a two-sided < 0.05 was considered statistically significant.
The positive expression rate and expression intensity of PEDF were gradually decreased in the normal control group, adenoma group, and CRC group (100% 78% 50%, = 34.430, < 0.001; ++++ +++ -+, = 94.059, < 0.001), while VEGF increased gradually (0% 68% 96%, = 98.35, < 0.001; - -+ ++~+++, = 107.734, < 0.001). In the CRC group, the positive expression rate of PEDF decreased with the increase of differentiation degree, invasion depth, lymph node metastasis, distant metastasis, and TNM stage ( = 20.513, 4.160, 5.128, 6.349, 5.128, < 0.05); the high expression rate of VEGF was the opposite ( = 10.317, 13.134, 17.643, 21.844, 17.643, < 0.05). In the colorectal adenoma group, the expression intensity of PEDF correlated negatively with CD31-MVD ( = -0.601, < 0.001), whereas VEGF was not significantly different ( = 0.258, = 0.07). In the CRC group, the expression intensity of PEDF correlated negatively with the expression intensity of CD31-MVD and VEGF ( = -0.297, < 0.05; = -0.548, 0.05 while VEGF expression intensity was positively related to CD31-MVD ( = 0.421, = 0.002).
It is possible that PEDF can be used as a new treatment and prevention target for CRC by upregulating the expression of PEDF while inhibiting the expression of VEGF.
结直肠癌(CRC)的发病率和死亡率位居世界前列,其发生发展与肿瘤新生血管形成密切相关。当抑制血管生成的色素上皮衍生因子(PEDF)与刺激血管生成的血管内皮生长因子(VEGF)之间的平衡被打破时,血管生成失控,导致肿瘤发展。因此,寻找更多CRC的治疗靶点以进行早期干预和后续治疗非常必要。
探讨PEDF、VEGF及CD31染色微血管密度值(CD31-MVD)在正常结直肠黏膜、腺瘤及CRC中的表达及意义。
在本病例对照研究中,收集了成都第二人民医院消化内镜中心和普通外科2022年4月至2022年10月的存档标本蜡块。选取50例经电子结肠镜及同步活检确诊为正常肠黏膜的标本蜡块作为正常对照组,50例经电子结肠镜及病理活检确诊为结直肠腺瘤的标本蜡块作为腺瘤组,50例经普通外科住院手术后病理活检确诊为CRC的标本蜡块作为CRC组。进行免疫组织化学染色实验检测三组标本中PEDF和VEGF的表达,分析其差异,研究CRC组中二者与临床病理因素的关系,记录三组的CD31-MVD,并分析结直肠腺瘤组和CRC组中PEDF、VEGF及CD31-MVD的相关性。计量资料采用t检验或校正t检验进行统计学分析。等级资料组间比较采用Kruskal-Wallis秩和检验。组间率的比较采用卡方检验、校正卡方检验或Fisher确切概率法。组间所有差异均采用Bonferroni法进行多重比较。采用Spearman相关分析检验数据的相关性。检验水准(α)为0.05,双侧P<0.05认为差异有统计学意义。
正常对照组、腺瘤组及CRC组中PEDF的阳性表达率及表达强度逐渐降低(100%>78%>50%,χ²=34.430,P<0.001;+++++>+++>-+,χ²=94.059,P<0.001),而VEGF逐渐升高(0%<68%<96%,χ²=98.35,P<0.001;-<-+<++~+++,χ²=107.734,P<0.001)。在CRC组中,PEDF的阳性表达率随分化程度、浸润深度、淋巴结转移、远处转移及TNM分期的增加而降低(χ²=20.513、4.160、5.128、6.349、5.128,P<0.05);VEGF的高表达率则相反(χ²=10.317、13.134、17.64