Expression of HER2/neu in gastric adenocarcinoma and its correlation with serum HER2/neu level and E-cadherin expression

被引:4
作者
Pandey, Ishan [1 ]
Misra, Vatsala [1 ]
Pandey, Aprajita T. [2 ]
Verma, Amita [3 ]
机构
[1] Moti Lal Nehru Med Coll, Dept Pathol, Prayagraj 211001, Uttar Pradesh, India
[2] Univ Allahabad, Ctr Biotechnol, Prayagraj, Uttar Pradesh, India
[3] SHUATS, Dept Pharmaceut Sci, Bioorgan & Med Chem Res Lab, Prayagraj, Uttar Pradesh, India
关键词
E-cadherin; gastric adenocarcinoma; HER2/neu; immunohistochemistry; serum ELISA; CANCER; BREAST; VALIDATION;
D O I
10.4103/ijpm.ijpm_133_21
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Aim: To assess HER2/neu expressions and correlate with E-cadherin and Serum HER2 level in gastric carcinoma. Method: 31 gastric biopsies and 1 resected specimen were taken in the study with patient details and stained with H and E for histopathological details following Lauren's classification. Immunohistochemistry for HER2 and E-cadherin expression was conducted followed by serum HER2/neu ELISA. Result: Adenocarcinoma with 61% diffuse, 29% intestinal, and 10% other type were observed with predominant HER2 immunoexpression in intestinal-type than in diffuse-type adenocarcinoma. Other observations marked 44% as 3+/positive and 56% as 2+/equivocal in intestinal type while 26% cases as 3+/positive, 69% as 2+/equivocal, and 1% as 1+/negative were observed in diffuse type. The data presented 33% membranous positivity and 67% both membranous + cytoplasmic positivity in intestinal type while 2% showed membranous positivity, 47% both membranous + cytoplasmic, and 42% only cytoplasmic positivity in diffused type. On comparing the localization pattern of HER2 and E-cadherin, 25% of cases showed membranous staining while 50% of cases showed membranous with cytoplasmic staining for both. No cytoplasmic HER2 staining as well as no any staining for E-cadherin was shown by 6% cases. Conclusion: Thus, it can be concluded that cytoplasmic expression of HER2 in gastric adenocarcinoma (mainly diffuse type) may be due to shedding of its extracellular domain, leading to loss of membranous E-cadherin expression on immunohistochemistry. The loss of membranous expression of E-cadherin and increased serum HER2 ELISA were correlated well with these findings.
引用
收藏
页码:35 / 41
页数:7
相关论文
共 27 条
[1]  
[Anonymous], 2014, Int
[2]  
Bang YJ, 2010, LANCET, V376, P1302
[3]   HER2 testing in the UK: recommendations for breast and gastric in-situ hybridisation methods [J].
Bartlett, J. M. S. ;
Starczynski, J. ;
Atkey, Neil ;
Kay, E. ;
O'Grady, A. ;
Gandy, Michael ;
Ibrahim, Merdol ;
Jasani, Bharat ;
Ellis, I. O. ;
Pinder, S. E. ;
Walker, R. A. .
JOURNAL OF CLINICAL PATHOLOGY, 2011, 64 (08) :649-653
[4]   Cytoplasmic Overexpression of HER2: a Key Factor in Colorectal Cancer [J].
Blok, Erik J. ;
Kuppen, Peter J. K. ;
van Leeuwen, Jeroen E. M. ;
Sier, Cornelis F. M. .
CLINICAL MEDICINE INSIGHTS-ONCOLOGY, 2013, 7 :41-51
[5]  
Bosman F. T., 2010, WHO classification of tumours of the digestive system
[6]  
Cislo Magdalena, 2018, Oncotarget, V9, P19427, DOI 10.18632/oncotarget.24827
[7]   Cancer mortality in India: a nationally representative survey [J].
Dikshit, Rajesh ;
Gupta, Prakash C. ;
Ramasundarahettige, Chinthanie ;
Gajalakshmi, Vendhan ;
Aleksandrowicz, Lukasz ;
Badwe, Rajendra ;
Kumar, Rajesh ;
Roy, Sandip ;
Suraweera, Wilson ;
Bray, Freddie ;
Mallath, Mohandas ;
Singh, Poonam K. ;
Sinha, Dhirendra N. ;
Shet, Arun S. ;
Gelband, Hellen ;
Jha, Prabhat .
LANCET, 2012, 379 (9828) :1807-1816
[8]   Estimating the global cancer incidence and mortality in 2018: GLOBOCAN sources and methods [J].
Ferlay, J. ;
Colombet, M. ;
Soerjomataram, I. ;
Mathers, C. ;
Parkin, D. M. ;
Pineros, M. ;
Znaor, A. ;
Bray, F. .
INTERNATIONAL JOURNAL OF CANCER, 2019, 144 (08) :1941-1953
[9]  
Gill MK, 2011, J CLIN DIAGN RES, V5, P1564
[10]   HER-2 receptor expression, localization, and activation in colorectal cancer cell lines and human tumors [J].
Half, E ;
Broaddus, R ;
Danenberg, KD ;
Danenberg, PV ;
Ayers, GD ;
Sinicrope, FA .
INTERNATIONAL JOURNAL OF CANCER, 2004, 108 (04) :540-548