PR, Cell Lines, Cancer

The availability of genetically defined reference materials, offers an industry standard for development and quality control of IHC assays, directly, thereby improving the accuracy and reproducibility. Using engineered cell lines as quality control material to assess the performance of IHC assays eliminates the variability associated with patient-derived reference standards.

This APP can be used for quality control of PR strong positive, intermediate positive and negative cell line material to ensure that each cell line block complies with the expected PR expression before the material is used as reference standard for IHC assays. The APP quantifies the PR expression in each cell line core and relates this expression to a known reference value for each cell line expression level.

Figure 1

Raw image of cell line cores with different PR expression.

Figure 2

Zoomed in image of the strong positive cell line core. Primarily nuclei with a strong positive expression are present.

Figure 3

The image from FIGURE 2, analyzed with the APP. Strong positive nuclei (3+) are labeled red, intermediate nuclei (2+) orange, weak nuclei (+1) yellow, and negative nuclei blue.

Figure 4

Intermediate positive cell line core, demonstrating a variation of staining.

Figure 5

The analyzed intermediate cell line core in FIGURE 4, demonstrating the detection of the varying staining intensity. Strong positive nuclei (3+) are labeled red, intermediate (2+) orange, weak (+1) yellow, and negative blue.

Figure 6

Negative cell line core.

Figure 7

The analyzed negative cell line core in FIGURE 6.

Details

Quantitative Output variables

The output variables obtained from this protocol are:

Neg Nuclei (#): The number of negative nuclei.
1+ Nuclei (#): The number of 1+ classified nuclei.
2+ Nuclei (#): The number of 2+ classified nuclei.
3+ Nuclei (#): The number of 3+ classified nuclei.
Positive Percentage: The percentage of positive nuclei profiles.
H-score: (Percentage of 3+) x 3 + (Percentage of 2+) x 2 + (Percentage of 1+).
Category: 0 if the cell line core is negative according to the reference H-score level for the PR negative cell line cores, 1 if the cell line core is intermediate positive according to the reference H-score level for PR intermediate cell line cores, and 2 if the cell line core is positive according to the reference H-score level for PR positive cell line cores.

Methods

The first image processing step involves a segmentation of all nuclei in the ROI. This is done by using an HDAB-DAB color deconvolution band to detect positively stained nuclei and the Haematoxylin-HDAB color deconvolution band to detect negative nuclei. 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. Then the positive nuclei are subdivided into three categories based on staining intensities. As a post-processing step, nuclei areas that are too small are removed. The image obtained after post-processing, see FIGURE 3, is used for quantifying the PR expression in each cell line core based on the H-score. As a final step the H-score is related to a known reference value for each cell line expression level.

Staining Protocol

There is no staining protocol available.

Keywords

Progesteron receptor, cell line, quality control, reference standards, image analysis.

References

USERS
The APP was developed for Horizon cell lines.

LITERATURE
There are currently no references.