Monoclonal Antibodies Against Breast Cancer

Coinciding with the world day of the fight against breast cancer , we wanted to analyze the impact that relatively new biological therapies, especially monoclonal antibodies , have had against breast cancer.

One of the greatest advances made in recent years stems from knowledge of the different biological subtypes of breast cancer . Each of these profiles is susceptible of being treated with specific therapeutic resources, which allows administering personalized treatment in each case that is more effective and less aggressive.

In this sense, antitumor agents with more specific action on tumor cells have been developed in order to increase their efficacy and avoid their toxicity as much as possible by reducing the effects on healthy cells of traditional chemotherapy treatments.

Monoclonal antibodies against breast cancer , far from replacing chemotherapy drugs, are nowadays an adjuvant therapy that has shown beneficial effects in cases of tumors with more aggressive pathophysiological characteristics.

In this entry we collect monoclonal antibodies against breast cancer approved to date for therapeutic use in this pathology.

Monoclonal Antibodies As Antitumor Drugs

The effectiveness of monoclonal antibodies against breast cancer depends directly on the antigenic expression of tumor cells. In this sense, the target antigen must be specific to tumor cells, express itself at high levels, must not detach from the cell surface and must be accessible.

Monoclonal antibodies against breast cancer act through different mechanisms of action, including:

  • Opsonization
  • Activation of the complement system
  • Cytotoxicity
  • Target antigen blocking

In addition, the most innovative therapies conjugate drugs to monoclonal antibodies whose specificity transports them to cancer cells, thus increasing the efficacy of these drugs and reducing their toxicity.

Monoclonal Antibodies As Antitumor Drugs

Currently, there are 4 monoclonal antibodies against breast cancer whose therapeutic use is authorized by health authorities.


Trastuzumab was the first monoclonal antibody against breast cancer to be licensed nearly 2 decades ago.

It is a humanized monoclonal antibody of the IgG1 type, against the human epidermal growth factor receptor 2 (HER-2). The HER-2 receptor is overexpressed in 20-30% of breast cancer cases, causing a faster proliferation of the tumor and greater aggressiveness.

Trastuzumab inhibits cell proliferation of HER-2 positive tumors through two main mechanisms of action:

  • Binding of trastuzumab to the overexpressed receptor inhibits signaling via the phosphatidylinositol-3-kinase pathway, and as a consequence, inhibits tumor cell proliferation.
  • It is a strong mediator of antibody-dependent cytotoxicity.

Bevacizumab was the second antibody to be licensed to expand the therapeutic arsenal against breast cancer.

In this case, it is a monoclonal antibody against vascular endothelial growth factor ( VEGF ) . This antibody binds to all isoforms of this factor, blocking its binding to the biological receptors present on the surface of vascular endothelial cells.

The main mechanism of action is to block the binding of VEGF to its receptor, thus inhibiting tumor neovascularization, and consequently tumor growth.


Pertuzumab is one of the most recently licensed monoclonal antibodies against breast cancer.

It is a humanized monoclonal antibody of the IgG1 type, which, like Trastuzumab, specifically binds to receptor 2 for human epidermal growth factor (HER-2) , and acts through the same mechanism of action.


Trastuzumab-emtansine is a covalent conjugate of the monoclonal antibody trastuzumab with the cytotoxic agent DM1 , which was licensed for marketing just over two years ago.

The DM-1 chemotherapy, whose mechanism of action consists of the inhibition of tubulin polymerization, thus stopping the cell cycle and promoting apoptosis, acts selectively on HER-2 positive tumor cells thanks to its binding to trastuzumab. Upon binding of this antibody to the receptor, the complex is internalized in the cell releasing the cytotoxic metabolites inside the cell.

The monoclonal antibodies against breast cancer have been a breakthrough in the personalized and selective treatment for certain types of breast cancer and can specifically block the proliferation of tumors, and opening the door to the development of new drugs conjugated to direct chemotherapy selectively to tumor cells, thus making it more effective and less toxic.

How To Do An Sds-Page: Tips And Tricks

The SDS-PAGE gels are basic and commonly used technique in most research laboratories. Its use is aimed at separating the proteins present in a sample based on their molecular weight. This separation is based on the different speed of protein migration through a polyacrylamide gel when applying an electric field.

In this post we collect some tips and tricks on how to do an SDS-PAGE optimally.

1.- Prepare the reagents in advance . You can do it with all those that are likely to be stored and used for some time without deterioration.

  • Buffers: A concentrated solution can be prepared, and a small amount diluted for each experiment.
  • Ammonium persulfate: If it is to be used frequently, it can be stored at 4ºC for about a month. For longer periods of time it can be aliquoted and frozen at -20ºC.
  • Gels: Gels can also be prepared in advance and stored refrigerated (4ºC) for 10-15 days. In this case it is essential to ensure that they are kept moist until use.
  • Samples: They can be prepared and frozen at -20ºC for some months. In this way, once thawed, they will be ready for loading in the gel.

2.- Substitute the distilled water for isopropanol to cover the gel. This will allow the gel to polymerize faster.

3.- Be sure to maintain the proper buffer level in the wells. If the buffer volume drops too low, the wells will dry out and the gel will not run properly.

4.- Prepare the polyacrylamide gel based on the molecular weight of the proteins you are interested in separating. Proteins with higher molecular weights move more slowly through the pores of the gel. The size of these pores can be modulated depending on the size of the proteins to be separated, changing the concentration of polyacrylamide according to the following indicative ranges:

Molecular weight ofproteins to separate% polyacrylamide
3-100 kDafifteen%
10-200 kDa12%
20-300 kDa10%
50-500 kDa7%

For protein mixtures with a higher molecular weight range, gradient gels with layers of increasing concentration of polyacrylamide can be used.

5.- If you are running sensitive samples (for example protein-RNA complexes), spray the plates with ethanol (70%) and DEPC water (diethylpyrocarbonate), and make sure they are well dry before starting.

6.- Be careful with the electric power . Although the higher the migration speed of the samples increases, the probability of overheating the gel also increases. To avoid this, consult the manufacturer’s instructions and adjust to the recommended voltage.

7.- High or irregular temperatures throughout the gel directly affect the migration of the samples. There are several ways to keep the temperature low , including filling the outside of the tank with the buffer to the bottom of the wells so that the heat is dispersed evenly throughout the gel.