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Metabolic Imaging as a Tool to Characterize Chemoresistance and Guide Therapy in Triple-Negative Breast Cancer (TNBC).

Publication ,  Journal Article
Sunassee, ED; Jardim-Perassi, BV; Madonna, MC; Ordway, B; Ramanujam, N
Published in: Molecular cancer research : MCR
October 2023

After an initial response to chemotherapy, tumor relapse is frequent. This event is reflective of both the spatiotemporal heterogeneities of the tumor microenvironment as well as the evolutionary propensity of cancer cell populations to adapt to variable conditions. Because the cause of this adaptation could be genetic or epigenetic, studying phenotypic properties such as tumor metabolism is useful as it reflects molecular, cellular, and tissue-level dynamics. In triple-negative breast cancer (TNBC), the characteristic metabolic phenotype is a highly fermentative state. However, during treatment, the spatial and temporal dynamics of the metabolic landscape are highly unstable, with surviving populations taking on a variety of metabolic states. Thus, longitudinally imaging tumor metabolism provides a promising approach to inform therapeutic strategies, and to monitor treatment responses to understand and mitigate recurrence. Here we summarize some examples of the metabolic plasticity reported in TNBC following chemotherapy and review the current metabolic imaging techniques available in monitoring chemotherapy responses clinically and preclinically. The ensemble of imaging technologies we describe has distinct attributes that make them uniquely suited for a particular length scale, biological model, and/or features that can be captured. We focus on TNBC to highlight the potential of each of these technological advances in understanding evolution-based therapeutic resistance.

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Published In

Molecular cancer research : MCR

DOI

EISSN

1557-3125

ISSN

1541-7786

Publication Date

October 2023

Volume

21

Issue

10

Start / End Page

995 / 1009

Related Subject Headings

  • Tumor Microenvironment
  • Triple Negative Breast Neoplasms
  • Oncology & Carcinogenesis
  • Neoplasm Recurrence, Local
  • Humans
  • Drug Resistance, Neoplasm
  • Developmental Biology
  • 3211 Oncology and carcinogenesis
  • 3101 Biochemistry and cell biology
  • 1112 Oncology and Carcinogenesis
 

Citation

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Sunassee, E. D., Jardim-Perassi, B. V., Madonna, M. C., Ordway, B., & Ramanujam, N. (2023). Metabolic Imaging as a Tool to Characterize Chemoresistance and Guide Therapy in Triple-Negative Breast Cancer (TNBC). Molecular Cancer Research : MCR, 21(10), 995–1009. https://doi.org/10.1158/1541-7786.mcr-22-1004
Sunassee, Enakshi D., Bruna Victorasso Jardim-Perassi, Megan C. Madonna, Bryce Ordway, and Nirmala Ramanujam. “Metabolic Imaging as a Tool to Characterize Chemoresistance and Guide Therapy in Triple-Negative Breast Cancer (TNBC).Molecular Cancer Research : MCR 21, no. 10 (October 2023): 995–1009. https://doi.org/10.1158/1541-7786.mcr-22-1004.
Sunassee ED, Jardim-Perassi BV, Madonna MC, Ordway B, Ramanujam N. Metabolic Imaging as a Tool to Characterize Chemoresistance and Guide Therapy in Triple-Negative Breast Cancer (TNBC). Molecular cancer research : MCR. 2023 Oct;21(10):995–1009.
Sunassee, Enakshi D., et al. “Metabolic Imaging as a Tool to Characterize Chemoresistance and Guide Therapy in Triple-Negative Breast Cancer (TNBC).Molecular Cancer Research : MCR, vol. 21, no. 10, Oct. 2023, pp. 995–1009. Epmc, doi:10.1158/1541-7786.mcr-22-1004.
Sunassee ED, Jardim-Perassi BV, Madonna MC, Ordway B, Ramanujam N. Metabolic Imaging as a Tool to Characterize Chemoresistance and Guide Therapy in Triple-Negative Breast Cancer (TNBC). Molecular cancer research : MCR. 2023 Oct;21(10):995–1009.

Published In

Molecular cancer research : MCR

DOI

EISSN

1557-3125

ISSN

1541-7786

Publication Date

October 2023

Volume

21

Issue

10

Start / End Page

995 / 1009

Related Subject Headings

  • Tumor Microenvironment
  • Triple Negative Breast Neoplasms
  • Oncology & Carcinogenesis
  • Neoplasm Recurrence, Local
  • Humans
  • Drug Resistance, Neoplasm
  • Developmental Biology
  • 3211 Oncology and carcinogenesis
  • 3101 Biochemistry and cell biology
  • 1112 Oncology and Carcinogenesis