Heterogeneity of drug resistance in human breast and ovarian cancers

D H Kern1

  • 1Oncotech, Inc., Irvine, CA 92714, USA.

The Cancer Journal From Scientific American
|February 19, 1998
PubMed
Abstract

Insights

Drug resistance varies significantly between tumor sites in breast and ovarian cancers, complicating chemotherapy. Understanding this drug resistance heterogeneity is crucial for effective cancer treatment.

Area of Science:

  • Oncology
  • Cancer Biology
  • Pharmacology

Background:

  • Drug resistance is a major challenge in treating advanced breast and ovarian cancers.
  • Tumor heterogeneity can lead to differential responses to chemotherapy agents.
  • Understanding resistance patterns is vital for personalized treatment strategies.

Purpose of the Study:

  • To quantify the extent of drug resistance heterogeneity in breast and ovarian cancers.
  • To identify drug-specific resistance patterns in tumors from multiple sites.
  • To provide insights into the unique biology of individual patient diseases.

Main Methods:

  • The extreme drug resistance (EDR) assay was used to measure resistance to cisplatin, paclitaxel, and doxorubicin.
  • Resistance was assessed in multiple synchronous or metachronous tumors.
  • Tumor resistance was classified into low drug resistance (LDR), EDR, or intermediate drug resistance (IDR) categories.

Main Results:

  • Significant heterogeneity in drug resistance was observed for cisplatin, paclitaxel, and doxorubicin across different tumor sites and recurrence.
  • Discordant resistance categories (e.g., EDR vs. LDR) were found in 4-24% of paired tumor samples.
  • Metastatic sites showed a slightly higher incidence of extreme drug resistance (EDR) compared to primary sites.

Conclusions:

  • Drug resistance heterogeneity is a significant clinical issue in managing metastatic and recurrent breast and ovarian cancers.
  • Recognizing this heterogeneity is the first step toward optimizing chemotherapy administration.
  • Drug resistance testing can guide physicians in selecting effective chemotherapeutic agents and avoiding resistant ones.

Related Concept Videos

Treatment Resistant Cancers02:56

Treatment Resistant Cancers

Cancer is the second leading cause of death in the United States. A cancer cell is genetically unstable and hence can mutate faster. They can also modify their microenvironment and escape immune surveillance. The difficulties in treating cancer are further compounded by the emergence of rapid resistance to anticancer drugs. The most common ways to attain resistance in cancer cells include alteration in drug transport and metabolism, modification of drug target, elevated DNA damage response, or...
Treatment Resistent Cancers02:56

Treatment Resistent Cancers

Cancer is the second leading cause of death in the United States. A cancer cell is genetically unstable and hence can mutate faster. They can also modify their microenvironment and escape immune surveillance. The difficulties in treating cancer are further compounded by the emergence of rapid resistance to anticancer drugs. The most common ways to attain resistance in cancer cells include alteration in drug transport and metabolism, modification of drug target, elevated DNA damage response, or...
Pharmacogenetic Phenotypes: Alterations in Pharmacokinetics, Drug Targets and Biologic Milieu01:29

Pharmacogenetic Phenotypes: Alterations in Pharmacokinetics, Drug Targets and Biologic Milieu

Genetic variations significantly influence drug response through pharmacokinetics, receptor interactions, and biologic milieu modifications. Pharmacokinetic alterations impact drug metabolism and clearance, affecting efficacy and toxicity. Variants in drug-metabolizing enzymes, such as CYP2C9 and CYP2C19, alter drug activation and elimination. For example, CYP2C9 loss-of-function variants require lower warfarin doses to prevent excessive bleeding, while CYP2C19 variants reduce clopidogrel...