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10017 - PHH3+PCK, Breast Cancer

INTRODUCTION

This APP has been developed to quantify the mitotic index of PHH3 positive cells within breast carcinoma. The APP uses the Virtual Double Staining (VDS) technique, which enables automated and robust detection of tumor regions.

Two serial sections stained respectively for PHH3 and Pancytokeratin (PCK) must be used in this APP. Tumor regions are identified automatically on the PCK stained slide and the outlined tumor region is overlaid on the PHH3 stained slide, thus automatically identifying tumor regions. 

Phosphohistone H3 (PHH3) is a mitotic marker and has prognostic capabilities when applied to breast cancer tissue [See REFERENCES: 3]. The mitotic index can be obtained by PHH3-immunohistochemical staining, which can be used as a supplement for diagnosis.

PCK is used as a cytoplasmatic marker to localize the cancer tissue.
This APP can be used to automatically outline tumor regions and determine the mitotic index. The APP described here is developed for TMA cores, but the method can easily be applied to whole slides as well.

KEYWORDS

VDS, Virtual Double Staining, breast carcinoma, PHH3, Phosphohistone, immunohistochemistry, breast cancer, quantitative, digital pathology, image analysis, PCK, Cytokeratin, mitotic index, TMA

METHODS

To employ the VDS approach for PHH3, two serial sections must be stained for PHH3 and PCK respectively.
This APP works as a three-step process as described below.

First, alignment of TMA cores from the two serial sections is performed [See EXAMPLES: figure 3]. The alignment is done both on a large, whole core scale, and on a finer detail level, to get the best possible match of the two tissue sections.

Second, tumor areas are automatically detected from the PCK slide and outlined as regions of interest (ROIs) [See EXAMPLES: figure 4]. The ROIs are then superimposed on the aligned PHH3 tissue slide to outline the tumor region for subsequent analysis limited to the inside of the tumor regions [See EXAMPLES: figure 5].

Finally, segmentation is performed of all nuclei on the PHH3 stained image inside the ROIs [See EXAMPLES: figure 6]. A method for nuclei separation which is based on shape, size and nuclei probability is used, employing a fully automated watershed-based nuclei segmentation technique. A post-processing step involving a morphological closing operation is applied to avoid counting nuclei in the late mitotic phase (anaphase and telophase) as two nuclei.
The number of positive PHH3 nuclei and the mitotic index are calculated.

QUANTITATIVE OUTPUT VARIABLES

The output variables obtained from this protocol include the number of positive nuclei profiles, the area of tumor tissue and the mitotic index. The mitotic index is calculated as follows: 

- NUC POS: number of positive nuclei profiles
- Mitotic index = NUC POS / Area of Tumor

AUXILIARY APPS (included)

Auxiliary APPs are used for additional process steps, e.g. finding Region of Interest (ROI).

Several auxiliary APPs are used for the final nuclei segmentation. These include: Tissue segmentation, Tissue alignment and ROI detection.

STAINING PROTOCOL

There is no staining protocol available

ADDITIONAL INFORMATION

This APP has been developed in cooperation with Professor Mogens Vyberg from NordiQC and Aalborg University Hospital Denmark and assistant professor Mette Christa Zeuthen from the Danish University College Metropol.

The APP utilizes the EngineTM and Viewer software modules, where EngineTM offers an execution platform to expand processing capability and speed of image analysis. Viewer gives a fast review together with several types of image adjustment properties ex. outlining of regions, annotations and direct measures of distance, curve length, radius, etc. 
By adding the AuthorTM module the APP can be customized to fit other purposes. AuthorTMoffers a comprehensive and dedicated set of tools for creating new fit-for-purpose analysis APPs, and no programming experience is required.

The APP also utilizes the module TissuealignTM, which gives the ability to align and subsequently analyze digitized serial sections. It also offers integrated VirtualDoubleStainingTM and VirtualMultiplexingTM.

REFERENCES

USERS


This APP was developed for, and validated by, Niels Fristrup MD and Dr. Lars Dyrskjøt Andersen, Center for Molecular Clinical Cancer Research Department of Molecular Medicine (MOMA) Aarhus University Hospital

LITTERATURE

1. Phosphohistone H3 expression has much stronger prognostic value than classical prognosticators in invasive lymph node-negative breast cancer patients less than 55 years of age, Ivar Skaland et al., Mod Pathol 20(12):1307-1315, October 2007.

2. Learning histopathological patterns, A. Kårsnäs, A. L. Dahl, R. Larsen, Journal of Pathology Informatics, 2(2):12, 2011

3. Segmenting Clustered Nuclei Using H-minima Transform-Based Marker Extraction and Contour Parameterization, C. Jung et al., IEEE Transactions on Biomedical Engineering 57(10): 2600-2604, 2010.

RUO
FIGURE 1
FIGURE 1
Original TMA-core stained with PCK.
FIGURE 2
FIGURE 2
Original TMA-core stained with PHH3.
FIGURE 3
FIGURE 3
Tissue alignment. The PCK and PHH3 TMA-cores are aligned to each other.
FIGURE 4
FIGURE 4
The cancer region is segmented in the PCK tissue and outlined with a ROI.
FIGURE 5
FIGURE 5
The ROI obtained from the PCK tissue is superimposed on the aligned PHH3 tissue. The ROI only outlines tumor regions. Tissue that is not tumor and the background are excluded.
FIGURE 6
FIGURE 6
Nuclei segmentation is performed only inside the tumor region. Green labels are positive PHH3 nuclei.