中山大学附属第一医院病理科,广东 广州 510080
缪娜波,硕士研究生,研究方向:淋巴瘤病理,E-mail: 994212891@qq.com
收稿:2020-02-29,
纸质出版:2020-07-15
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缪娜波,黎绮铭,李淑华等.p-AXL与c-MYC和/或BCL-2共表达在弥漫大B细胞性淋巴瘤中的临床意义[J].中山大学学报(医学科学版),2020,41(04):572-581.
MIAO Na-bo,LI Qi-ming,LI Shu-hua,et al.Clinical Significance of Expression of p-AXL and Co-expression with c-MYC and/or BCL-2 in DLBCL[J].Journal of Sun Yat-sen University(Medical Sciences),2020,41(04):572-581.
缪娜波,黎绮铭,李淑华等.p-AXL与c-MYC和/或BCL-2共表达在弥漫大B细胞性淋巴瘤中的临床意义[J].中山大学学报(医学科学版),2020,41(04):572-581. DOI:
MIAO Na-bo,LI Qi-ming,LI Shu-hua,et al.Clinical Significance of Expression of p-AXL and Co-expression with c-MYC and/or BCL-2 in DLBCL[J].Journal of Sun Yat-sen University(Medical Sciences),2020,41(04):572-581. DOI:
目的
2
探索磷酸化酪氨酸激酶p-AXL在弥漫大B细胞性淋巴瘤(DLBCL)中的表达情况及其临床病理意义,并进一步探讨p-AXL与c-MYC和/或BCL-2共表达的临床病理意义,及其与
MYC
断裂基因的临床病理联系。
方法
2
收集2012-2017年在中山大学附属第一医院确诊为DLBCL的病例118例,将入组的石蜡组织制作成组织芯片。免疫组化法检测DLBCL组织中p-AXL、c-MYC和BCL-2蛋白的表达;荧光原位杂交法(FISH)检测DLBCL组织中
MYC
断裂基因的表达情况。
结果
2
p-AXL蛋白在DLBCL肿瘤细胞的胞膜和/或胞质中表达;p-AXL表达与DLBCL化疗缓解呈显著性相关(
P
<0.01),阳性患者化疗缓解率低于阴性患者;p-AXL表达与Hans分型显著性相关(
P
<0.01),p-AXL多见于Non-GCB型;p-AXL与c-MYC、BCL-2及c-MYC/BCL-2蛋白表达均显著性相关(
P
<0.01)。p-AXL/c-MYC、p-AXL/BCL-2、p-AXL/c-MYC/BCL-2蛋白共表达均与Hans分型显著性相关(
P
<0.01),多见于Non-GCB型。p-AXL与患者无进展生存期(PFS)显著性相关,阳性者PFS低于阴性患者(
P
<0.05);p-AXL阳性者总生存期(OS)亦低于p-AXL阴性者,但差异未达统计学意义(
P
>0.05)。单变量分析显示,男性且p-AXL阳性、Non-GCB型且p-AXL阳性、p-AXL/c-MYC、p-AXL/c-MYC/BCL-2蛋白共表达均是DLBCL患者PFS和OS降低的危险因素(
P
<0.05);但是,多变量分析显示,仅男性且p-AXL阳性、p-AXL/c-MYC蛋白共表达是DLBCL患者PFS和OS降低的显著性危险因素(
P
<0.05
;P
<0.01)。
结论
2
DLBCL中p-AXL与c-MYC和/或BCL-2的表达、Hans分型、肿瘤化疗缓解率降低和PFS缩短均显著性相关;p-AXL/c-MYC共表达、男性且p-AXL阳性均可作为DLBCL的独立性预后指标。
Objective
2
To investigate the expression and significance of phosphorylated receptor tyrosine kinase(p-AXL)in diffuse large B cell lymphoma (DLBCL)
and the clinical value of its co-expression with BCL-2 and /or
c-MYC
split gene.
Methods
2
Totally 118 cases of DLBCL were collected in the First Affiliated Hospital of Sun Yat-sen University from 2012 to 2017,and prepared as tissue array. p-AXL
c-MYC and BCL-2 proteins were detected by immunohistochemistry
and c-MYC split gene was detected by FISH staining.
Results
2
p-AXL protein was stained on tumor cells’ membrane or in the cytoplasm of DLBCL cells. p-AXL was expressed more commonly in Non-GCB type than in GCB type. The expression of p-AXL was significantly correlated with the chemotherapy effect (
P
<
0.01)
and the expression of
c-MYC
split gene or BCL-2 protein separately (
P
<
0.01). Co-expression of p-AXL and c-MYC
or BCL-2
or both of them was significantly correlated with the Hans typing (
P
<
0.01). The PFS of p-AXL positive patients was obviously lower than that of p-AXL negative patients (
P
<
0.05). The OS of p-AXL positive patients was also lower than that of the negative patients
but the difference had no statistical significance (
P
>
0.05). Univariate analysis showed that p-AXL and male
p-AXL and Non-GCB type
p-AXL and c-MYC co-expression
p-AXL and c-MYC and/or BCL-2 co-expression were the risk factors for PFS and OS in DLBCL patients (
P
<
0.05). Multivariate analysis showed that p-AXL positive in male (
P
<
0.05) and p-AXL/c-MYC co-expression (
P
<
0.01) were independent risk factors for PFS and OS in DLBCL patients.
Conclusions
2
p-AXL protein is expressed in DLBCL
and its expression is significantly related to the expression of c-MYC and BCL-2. p-AXL expression is associated with lower chemotherapy response rate
shorter progression-free survival and shorter overall survival. p-AXL/c-MYC co-expression or p-AXL positive in male may be an independent prognostic factor for DLBCL patients.
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