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Breast Cancer

Breast cancer is a complex and challenging disease that affects a significant number of women worldwide. At Alfa Cytology, we are committed to helping our clients unravel the complexity of these diseases by providing integrated preclinical research solutions.

Introduction to Breast Cancer

Breast cancer is the most common non-cutaneous malignancy in women, both in Europe and the United States, and ranks as the second leading cause of cancer-related deaths. Understanding the various aspects of breast cancer, including its types and current therapeutic strategies, is crucial in the fight against this formidable disease.

Introduction to Breast Cancer.Fig.1 Breast Cancer Frequency, 1975-2019, Age & Sex. (Milano, A. F., 2023)

Types of Breast Cancer

Breast cancers are classified into four subtypes based on risk, prognosis, and likelihood of response to treatment: luminal A, luminal B, HER2 overexpressing, and triple-negative (Basal-like). Luminal is characterized by the expression of oestrogen receptor (ER) and progesterone receptor (PR), as well as other related genes; the HER2 gene is amplified in about 15% of invasive Breast cancer is amplified. Basal, on the other hand, expresses epithelial genes in large quantities, such as cytokeratins 5 and 17, but with some loss of expression of ER, PR and HER2.

Types of Breast Cancer.Fig.2 Types of Breast Cancer.

Therapy Development for Breast Cancer

Targets Current Therapies
Key cell surface receptors
  • Anti-HER2 monoclonal antibodies (trastuzumab, pertuzumab, and margetuximab)
  • Antibody-drug conjugates (ADCs), trastuzumab emtansine (T-DM1), and trastuzumab deruxtecan (T-DXd)
Trop2
  • ADCs (sacituzumab govitecan)
PD-L1
  • Atezolizumab, durvalumab, and avelumab
CTLA-4
  • Ipilimumab and tremelimumab
HER2
  • Tyrosine kinase inhibitors such as lapatinib, neratinib, and tucatinib.
MEK, PI3K, and AKT
  • MEK, PI3K, and AKT inhibitors are under investigation.
ER modulators (SERMS) or aromatase inhibitors (AIs)
  • Block estradiol production for ER+ breast cancer.
PARP
  • The targeting of single-strand DNA breaks in BRCA1/BRCA2 mutation carriers with PARP inhibitors is in clinical practice.

Our Services

At Alfa Cytology, our state-of-the-art preclinical research facilities and specialized team of biologists and scientists are dedicated to conducting groundbreaking in vitro and in vivo studies to explore novel therapeutic approaches, validate potential biomarkers, and uncover the underlying mechanisms of these complex diseases.

Our preclinical services encompass a wide range of capabilities, including cell line development, high-throughput screening, pharmacokinetic and pharmacodynamic evaluations, and advanced animal models.

Our Breast Cancer Modeling Services

  • Breast Cancer Cell Line Transplantation Model
    Species Cell Types Cell Line Oestrogen Receptor (ER) Progesterone Receptor (PR) HER2 Gene
    Homo sapiens (Human) Human breast adenocarcinoma cells MCF-7;
    MCF-7-LUC&GFP
    + + -
    MDA-MB-231;
    MDA-MB-231-LUC&GFP
    - - -
    MDA-MB-468 - - -
    ZR-75-1 + +/- -
    BT474 + + +
    Human mammary gland adenocarcinoma cells SK-BR-3(SKBR3);
    SK-BR-3-LUC&GFP
    - - +
    Human mammary ductal carcinoma cells T-47D + + -
    Rodent Mouse breast cancer cells 4T1;
    4T-1-LUC
    - - -
    EMT-6 - - -
  • Induced Models
    The inducible breast cancer model mostly adopts the chemical inducible pathway, and the commonly used inducing agents include methylnitrosourea (N-methyl-N-nitrosourea, MNU) or MCA, etc.

At Alfa Cytology, we are committed to the research and study of breast cancer, from molecular biology services, and cancer biomarker discovery services, to preclinical research services, providing one-stop services. For more information about our breast cancer research and development initiatives, or to inquire about our comprehensive services, please don't hesitate to contact us.

Reference

  1. Milano, A. F. (2023). Breast Cancer: 20-Year Comparative Mortality and Survival Analysis by Age, Sex, Race/Ethnicity, Stage, Grade, Disease Duration, Selected ICD-O-3 Oncophenotypes, and Cohort Entry Time-Period: A Systematic Review of 656,501 Cases for Diagnosis Years 1975-2019:(SEER* Stat 8.4. 0.1). Journal of Insurance Medicine, 50(2), 80-122.

! For research use only.