MCM7 (MSVA-507R)

The MCM7 gene is located at 7q22.1 and codes for a 80kDa protein which belongs to the highly conserved mini-chromosome maintenance proteins (MCM) 2-7 that play a key role in genome replication. They form a ring-shaped hexameric protein complex which is essential for the pre-replication complex and may be involved in the formation of replication forks, the recruitment of other DNA replication related proteins, and in maintaining genome integrity. Although uncomplexed MCM7 does not have ATPase or DNA helicase activity, it plays a role for DNA helicase activity of the MCM complex. MCM7 expression is regulated by E2F transcription factors under growth factor stimulation by PI3K/AKT, GSK3B , CCND1, and RB1. The MCM proteins are expressed in all cells in the G1, S, G2 and M-phase of the cell cycle but in contrast to the better established proliferation marker Ki-67, MCMs are already expressed in early G1 phase. This results in the detection of more proliferating cells as compared to Ki67 immunohistochemistry which might be advantageous in tumor types with low proliferative activity.

A nuclear MCM7 immunostaining of variable intensity – mostly strong – occurs in the cell compartments of tissues known to contain proliferating cells. This includes suprabasal and (weaker) basal cell layers of squamous epithelium and urothelium, mucous neck cells of the stomach, crypts of the intestine, as well as a fraction of epithelial cells of the gallbladder, respiratory epithelium and the fallopian tube. In the endometrium, almost all epithelial cells and many stromal cells are MCM7 positive but the rate of positive cells decreases in the secretion phase. A particularly strong MCM7 positivity occurs in most cells of germinal centres and the thymic cortex, and also in scattered individual cells all over the lymphatic tissues, while a large fraction of lymphocytes is at least weakly MCM7 positive. Almost all cells of the bone marrow are positive. In the testis, most spermatocytes are positive but mature sperms and probably also spermatogonia are negative. In the placenta, many cells of the cytotrophoblast and a fraction of stroma cells show strong MCM7 staining, while amnion and chorion cells are largely negative. Most granulosa cells and theca interna cells of the ovary exhibit at least a moderate positivity. A variable and often low number of MCM7 positive cells is seen in liver, pancreas, salivary glands, pituitary gland, thyroid, and parathyroid. Tissues and cell types with particularly low rate of MCM7 positive cells include prostatic luminal cells, seminal vesicle, and the endocervix.

A weak to moderate MCM7 staining can also be seen in most cells of several cell types which are known to not proliferate excessively. This includes heart (weak), skeletal (weak to moderate) and smooth muscle cells (negative to weak), and ovarian stroma cells (weak).

MCM7 is a ubiquitously expressed protein. The findings described above are this consistent with the RNA data described in the Human Protein Atlas (Tissue expression MCM7) 

Positive control = Colon: A strong nuclear MCM7 immunostaining should be seen in virtually all crypt base cells.

Negative control = Colon: MCM7 immunostaining should be largely absent in surface epithelial cells and in most stroma cells.

Normal tissue gallery

A nuclear MCM7 immunostaining in a fraction of tumor cells is always seen in cancerous tissues. 

The TCGA findings on MCM7 RNA expression in different tumor categories have been summarized in the Human Protein Atlas.

Cancer tissue gallery

No data available at the moment

IHC users have different preferences on how the stains should look like. Some prefer high staining intensity of the target stain and even accept some background. Others favor absolute specificity and lighter target stains. Factors that invariably lead to more intense staining include higher concentration of the antibody and visualization tools, longer incubation time, higher temperature during incubation, higher temperature and longer duration of the heat induced epitope retrieval (slide pretreatment). The impact of the pH during slide pretreatment has variable effects and depends on the antibody and the target protein.

All images and data shown here and in our image galleries are obtained by the manual protocol described below. Other protocols resulting in equivalent staining are described as well.

Manual protocol

Freshly cut sections should be used (less than 10 days between cutting and staining). Heat-induced antigen retrieval for 5 minutes in an autoclave at 121°C in pH 7,8 Target Retrieval Solution buffer. Apply MSVA-507R at a dilution of 1:150 at 37°C for 60 minutes. Visualization of bound antibody by the EnVision Kit (Dako, Agilent) according to the manufacturer’s directions.

Agilent / Dako – Autostainer Link 48

Pretreatment in PT-Link for 30 minutes at 95°C (pH high); FLEX peroxidase blocking for 5 minutes (room temperature), MSVA-507R 1:100 for 20 minutes (room temperature), FLEX+ mouse/rabbit (LINKER) for 15 minutes (room temperature), horseradish peroxidase (HRP) for 20 minutes (room temperature), FLEX DAB+Sub-Chromo for 10 minutes (room temperature), FLEX hematoxylin for 5 minutes (room temperature).

These images reflect stainings by the protocol described above. It is of note that a comparable staining result can also be obtained by different protocols. In general, a longer pretreatment, a longer incubation time of the primary antibody, a higher antibody concentration, and a longer incubation time of FLEX+LINKER result in stronger staining, potentially at the cost of more background staining. Modifications of the protocol with a strengthening effect on staining intensity in combination with changes of other parameters that result in lower staining intensity can result in a comparable result as shown above.

Leica – BOND RX

Dewax at 72°C for 30 seconds; Pretreatment in Bond Epitope Retrieval Solution (ER2 – EDTA pH9) for 20 minutes at 100°C; Peroxidase blocking for 5 minutes (room temperature), MSVA-507R 1:100 for 15 minutes (room temperature), Post primary (rabbit anti mouse) for 8 minutes (room temperature), Polymer (goat anti rabbit) for 8 minutes (room temperature), mixed DAB refine for 10 minutes (room temperature), hematoxylin for 5 minutes (room temperature).

These images reflect stainings by the protocol described above. It is of note that a comparable staining result can also be obtained by different protocols. In general, a longer pretreatment, a longer incubation time of the primary antibody, a higher antibody concentration, a higher temperature during incubation, and a longer incubation time of Post primary and or the Polymer result in stronger staining, potentially at the cost of more background staining. Modifications of the protocol with a strengthening effect on staining intensity in combination with changes of other parameters that result in lower staining intensity can result in a comparable result as shown above.

Roche – Ventana Discovery ULTRA

Pretreatment for 64 minutes at 100°C (pH 8,4); CM peroxidase blocking for 12 minutes (room temperature), MSVA-507R 1:150 for 20 minutes at 36°C, secondary antibody (anti-rabbit HQ) for 12 minutes at 36°C, anti-HQ HRP for 12 minutes at room temperature, DAB at room temperature, hematoxylin II at room temperature for 8 minutes, bluing reagent at room temperature for 4 minutes.

These images depict staining results obtained by the protocol described above. It is of note, that the Ventana machines generally require higher antibody concentrations than other commonly used autostainers because the antibodies are automatically diluted during the procedure. Various other protocols can result in an identical result as shown above. A longer pretreatment, a longer incubation time of the primary antibody, a higher antibody concentration, a higher temperature during incubation, and a longer incubation time of secondary antibody and or the anti-HQ HRP result in stronger staining, potentially at the cost of more background staining.

• Marker for proliferative cells.
• The prognostic role of the percentage of MCM7 positive cells is yet unknown for most tumor entities.
• It is unclear whether MCM7 quantification is equally or better suited than the established Ki67-LI for prognosis assessment.

In principle, there are two ways how the specificity of antibodies can be documented for immunohistochemistry on formalin fixed tissues. These are: 1. Comparison with a second independent method for target expression measurement across a large number of different tissue types (orthogonal strategy), and 2. Comparison with one or several independent antibodies for the same target and showing that all positive staining results are also seen with other antibodies for the same target (independent antibody strategy). 

For proteins such as MCM7 which are expressed in virtually all tissues but restricted to specific cell types and cell compartments, orthogonal validation is not well suited. However, the comparison of MSVA-507R immunostaining data with data from three independent RNA screening studies, including the Human Protein Atlas (HPA) RNA-seq tissue dataset, the FANTOM5 project, and the Genotype-Tissue Expression (GTEx) project, which are all summarized in the Human Protein Atlas (Tissue expression MCM7) supported the specificity of a weak MCM7 staining observed by MSVA-507R in virtually all cells of few tissue types with little proliferative activity such as heart, skeletal, and smooth muscle cells or ovarian stroma cells.

Comparison of antibodies: A specific staining of the MCM7 antibody MSVA-507R is supported by an identical staining pattern – mainly restricted to proliferating cell types – seen by employing the antibody CAB016312 (used for the analyses within the human protein atlas). The sensitivity of the assay used in the human protein atlas is lower than what is seen for MSVA-507R with the protocol suggested here. Accordingly, staining with CAB016312 is weaker and an unequivocal staining cannot be seen in heart and smooth muscle cells or ovarian stroma cells. However, some positive staining is visible for skeletal muscle. 

Normal tissue gallery