首页|ESYT3和FNDC1在肺腺癌中的表达及其与肿瘤进展关系

ESYT3和FNDC1在肺腺癌中的表达及其与肿瘤进展关系

扫码查看
目的 检测肺腺癌患者癌组织中扩展突触结合蛋白3(ESYT3)和Ⅲ型纤连蛋白结构域包含蛋白1(FNDC1)的表达,并分析两者与肿瘤进展的关系.方法 纳入2019-06-01-2022-06-01河南省胸科医院收治的137例肺腺癌患者病理组织标本.患者男96例,女41例;年龄43~76岁,平均年龄(65.87±8.14)岁.应用免疫组织化学染色法检测癌组织、癌旁组织(距离癌组织≥3 cm)ESYT3和FNDC1蛋白的阳性表达,分析其与临床病理特征的关系.随访截至2023-10-01,比较不同进展状态患者癌组织ESYT3和FNDC1阳性表达情况.采用x2检验分析ESYT3和FNDC1阳性表达与肺腺癌临床病理特征的关系,采用多因素Cox比例风险回归模型分析肺腺癌进展的影响因素,绘制Kaplan-Meier曲线分析癌组织ESYT3和FNDC1蛋白表达与肺腺癌进展的关系.结果 肺腺癌组织和癌旁组织中,ESYT3阳性表达率分别为33.58%(46/137)和 56.20%(77/137),FNDC1 阳性表达率分别为 43.07%(59/137)和 21.90%(30/137),差异均有统计学意义,x2值分别为14.177和13.995,均P<0.001.有吸烟史、TNM Ⅲ期、有淋巴结转移、未/低分化、胸膜侵袭患者,癌组织ESYT3阳性表达率分别低于无吸烟史(x2=7.344,P=0.007)、TNM Ⅰ/Ⅱ期(x2=7.766,P=0.005)、无淋巴结转移(x2=7.161,P=0.007)、中/高分化(x2=6.742,P=0.009)、无胸膜侵袭(x2=8.408,P=0.004)患者,癌组织FNDC1阳性表达率分别高于无吸烟史(x2=9.352,P=0.002)、TNM Ⅰ/Ⅱ期(x2=6.691,P=0.010)、无淋巴结转移(x2=4.258,P=0.039)、中/高分化(x2=7.421,P=0.006)、无胸膜侵袭(x2=7.738,P=0.005)患者.随访时间 16~52个月,中位随访时间37(18,48)个月,124例患者进展率50.81%(63/124).多因素Cox比例风险回归模型分析显示,吸烟史(HR=3.254,95%CI:1.339~7.908)、TNM Ⅲ期(HR=2.125,95%CI:1.279~3.531)、未/低分化(HR=2.032,95%CI:1.230~3.356)、癌组织 FNDC1 表达(HR=2.980,95%CI:1.570~5.657)是肺腺癌进展的危险因素,癌组织ESYT3表达(HR=0.961,95%CI:0.940~0.983)是其保护因素.癌组织ESYT3蛋白表达阳性和阴性患者的无进展生存时间(PFS)分别为51(95%CI:41.594~60.406)和43(95%CI:35.335~50.665)个月,差异有统计学意义,x2=6.294,P=0.012;癌组织FNDC1蛋白表达阳性和阴性患者PFS分别为39(95%CI:32.350~45.650)和48(95%CI:44.760~51.240)个月,差异有统计学意义,x2=8.075,P=0.004.结论 肺腺癌中ESYT3低表达,FNDC1高表达,两者与吸烟史、TNM分期、淋巴结转移、组织分化程度及胸膜侵袭相关,且是肺腺癌进展的影响因素.
Expression of ESYT3 and FNDC1 in lung adenocarcinoma and their relationship with tumor progression
Objective To detect the expression of extended synaptic binding protein 3(ESYT3)and type Ⅲ fibronectin do-main-containing protein 1(FNDC1)in lung adenocarcinoma patients,and to analyze their relationship with tumor progres-sion.Methods Pathological tissue specimens of 137 patients with lung adenocarcinoma admitted to Henan Chest Hospital from June 1,2019 to June 1,2022 were included.There were 96 males and 41 females.The average age was(65.87±8.14)years,ranging from 43 to 76 years.Immunohistochemical staining was used to detect the positive expression of ESYT3 and FNDC1 proteins in cancer tissues and adjacent tissues(≥3 cm from cancer tissues),and to analyze the relationship between the positive expression of ESYT3 and FNDC1 and clinicopathological features.The patients were followed up until October 1,2023 to compare the positive expression of ESYT3 and FNDC1 in cancer tissues of patients with different progression.x2 test was used to analyze the relationship between ESYT3 and FNDC1 positive expression and clinicopathological features of lung adenocarcinoma.Multi-factor Cox proportional risk regression model was used to analyze the influencing factors of lung adenocarcinoma progression,and Kaplan-Meier curve was plotted to analyze the re-lationship between ESYT3 and FNDC1 protein expression in cancer tissue and lung adenocarcinoma progression.Results The positive expression rates of ESYT3 and FNDC1 were 33.58%(46/137)and 56.20%(77/137)respectively in lung adenocarcinoma tissues and adjacent tissues,and the positive expression rates of FNDC1 were 43.07%(59/137)and 21.90%(30/137),respectively,with statistically significant differences,x2 value being 14.177 and 13.995,respec-tively,both P<0.001.The ESYT3 positive expression rate of patients with smoking history,TNM stage Ⅲ,lymph node metastasis,undifferentiated/poorly differentiated,and pleural invasion was lower than that of patients with no smoking history(x2=7.344,P=0.007),TNM stage Ⅰ/Ⅱ(x2=7.766,P=0.005),and no lymph node metastasis(x2=7.161,P=0.007),moderately/highly differentiated(x2=6.742,P=0.009),and no pleural invasion(x2=8.408,P=0.004);the positive expression rate of FNDC1 in cancer tissues was higher than that in patients with no his-tory of smoking(x2=9.352,P=0.002),TNM stage Ⅰ/Ⅱ(x2=6.691,P=0.010),and no lymph node metastasis(x2=4.258,P=0.039),moderately/highly differentiated(x2=7.421,P=0.006),and no pleural invasion(x2=7.738,P=0.005).The follow-up period ranged from 16 to 52 months,with a median follow-up time of 37(18,48)months.The progression rate of 124 patients was 50.81%(63/124).Multivariate Cox proportional hazard regression model analysis showed that smoking history(HR=3.254,95%CI:1.339-7.908),TNM stage Ⅲ(HR=2.125,95%CI:1.279-3.531),no/low differentiation(HR=2.032,95%CI:1.230-3.356),FNDC1 expression(HR=2.980,95%CI:1.570-5.657)were risk factors for the progression of lung adenocarcinoma,and ESYT3 expression(HR=0.961,95%CI:0.940-0.983)was a protective factor.The progression-free survival(PFS)of patients with posi-tive and negative ESYT3 protein expression was 51(95%CI:41.594-60.406)and 43(95%CI:35.335-50.665)months,respectively,and the difference was statistically significant(x2=6.294,P=0.012).The PFS of patients with positive and negative FNDC1 protein expression was 39(95%CI:32.350-45.650)and 48(95%CI:44.760-51.240)months,respectively,and the difference was statistically significant(x2=8.075,P=0.004).Conclusion The low ex-pression of ESYT3 and high expression of FNDC1 in lung adenocarcinoma are related to smoking history,TNM stage,lymph node metastasis,tissue differentiation degree and pleural invasion,and they are influencing factors for the progres-sion of lung adenocarcinoma.

lung adenocarcinomaextended synaptotagmin 3(ESYT3)fibronectin type Ⅲ domain-containing protein 1(FNDC1)tumor progression

马小杰、董庆芬、刘娟、李希婷、祁敏现

展开 >

河南省胸科医院病理科,河南郑州 450008

山东颐养健康集团新汶中心医院肿瘤科,山东泰安 271200

肺腺癌 扩展突触结合蛋白3 Ⅲ型纤连蛋白结构域包含蛋白1 肿瘤进展

2024

中华肿瘤防治杂志
中华预防医学会 山东省肿瘤防治研究院

中华肿瘤防治杂志

CSTPCD北大核心
影响因子:1.292
ISSN:1673-5269
年,卷(期):2024.31(19)