» Articles » PMID: 19123950

HER-2/neu Amplification Testing in Breast Cancer by Multiplex Ligation-dependent Probe Amplification: Influence of Manual- and Laser Microdissection

Overview
Journal BMC Cancer
Publisher Biomed Central
Specialty Oncology
Date 2009 Jan 7
PMID 19123950
Citations 13
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Accurate assessment of HER-2/neu status is crucial for proper prognostic information and to offer direct appropriate treatment for breast cancer patients. Next to immunohistochemistry (IHC) to evaluate HER2 protein overexpression, a second line gene amplification test is generally deemed necessary for cases with equivocal protein expression. Recently, a new PCR based test, called Multiplex Ligation-dependent Probe Amplification (MLPA), was introduced as a simple and quick method to assess HER-2/neu gene amplification status in invasive breast cancer. MLPA was previously shown to correlate well with IHC and in situ hybridization (ISH), but a low tumor percentage in the tissue tested could negatively affect the accuracy of MLPA results.

Methods: To examine this, MLPA was repeated in 42 patients after serial H&E section guided manual dissection with a scalpel and after laser microdissection of the tumor.

Results: Both dissection techniques led to higher HER2 gene copy number ratios and thereby made MLPA more quantitative. Concordance between MLPA and ISH improved from 61% to 84% after manual microdissection and to 90% after laser microdissection.

Conclusion: Manual and laser microdissection similarly increase the dynamic range of MLPA copy number ratios which is a technical advantage. As clinically a dichotomization between normal and amplified suffices and MLPA is relatively unsensitive to tumor content, microdissection before MLPA may not be routinely necessary but may be advisable in case of very low tumor content (<or=30%), when MLPA results are equivocal, or when extensive ductal carcinoma in situ is present. Since differences between manual and laser microdissection were small, less time consuming manual microdissection appears to be sufficient.

Citing Articles

Piezoelectric Ultrasonic Biological Microdissection Device Based on a Novel Flexure Mechanism for Suppressing Vibration.

Huang H, Pan Y, Pang Y, Shen H, Gao X, Zhu Y Micromachines (Basel). 2021; 12(2).

PMID: 33668595 PMC: 7918422. DOI: 10.3390/mi12020196.


Chromosome 17 copy number changes in male breast cancer.

Lacle M, Moelans C, Kornegoor R, van der Pol C, Witkamp A, van der Wall E Cell Oncol (Dordr). 2015; 38(3):237-45.

PMID: 25906114 PMC: 4445249. DOI: 10.1007/s13402-015-0227-7.


Quantification of HER family receptors in breast cancer.

Nuciforo P, Radosevic-Robin N, Ng T, Scaltriti M Breast Cancer Res. 2015; 17:53.

PMID: 25887735 PMC: 4389676. DOI: 10.1186/s13058-015-0561-8.


Multiplex Ligation-dependent Probe Amplification Can Clarify HER2 Status in Gastric Cancers with "Polysomy 17".

Wang T, Amemiya Y, Henry P, Seth A, Hanna W, Hsieh E J Cancer. 2015; 6(5):403-8.

PMID: 25874002 PMC: 4392047. DOI: 10.7150/jca.11424.


Determination of HER2 amplification status on tumour DNA by digital PCR.

Garcia-Murillas I, Lambros M, Turner N PLoS One. 2014; 8(12):e83409.

PMID: 24386193 PMC: 3873285. DOI: 10.1371/journal.pone.0083409.


References
1.
Purnomosari D, Aryandono T, Setiaji K, Nugraha S, Pals G, van Diest P . Comparison of multiplex ligation dependent probe amplification to immunohistochemistry for assessing HER-2/neu amplification in invasive breast cancer. Biotech Histochem. 2006; 81(2-3):79-85. DOI: 10.1080/10520290600822198. View

2.
Slamon D, Clark G, Wong S, Levin W, Ullrich A, McGuire W . Human breast cancer: correlation of relapse and survival with amplification of the HER-2/neu oncogene. Science. 1987; 235(4785):177-82. DOI: 10.1126/science.3798106. View

3.
Moelans C, de Weger R, van Blokland M, Ezendam C, Elshof S, Tilanus M . HER-2/neu amplification testing in breast cancer by multiplex ligation-dependent probe amplification in comparison with immunohistochemistry and in situ hybridization. Cell Oncol. 2008; 31(1):1-10. PMC: 4618800. DOI: 10.3233/clo-2009-0461. View

4.
Popescu N, King C, Kraus M . Localization of the human erbB-2 gene on normal and rearranged chromosomes 17 to bands q12-21.32. Genomics. 1989; 4(3):362-6. DOI: 10.1016/0888-7543(89)90343-1. View

5.
Pauletti G, Dandekar S, Rong H, Ramos L, Peng H, Seshadri R . Assessment of methods for tissue-based detection of the HER-2/neu alteration in human breast cancer: a direct comparison of fluorescence in situ hybridization and immunohistochemistry. J Clin Oncol. 2000; 18(21):3651-64. DOI: 10.1200/JCO.2000.18.21.3651. View