Susan Frost

Prof. Susan Frost

orcid

Research Focus & Metrics

Academic Career Length

35Years (1992-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 March 2008 in Plant Physiology
Verified
Journal Article
Closed access
SFSusan Frost
Susan Frost
MMMark C. Mescher
Mark C. Mescher
JCJohn E. Carlson
John E. Carlson
CMConsuelo M. De Moraes
Consuelo M. De Moraes

26 April 2007 in Ecology Letters
Verified
Journal Article
Closed access
PDF file
SFSusan Frost
Susan Frost
HAHeidi M. Appel
Heidi M. Appel
JCJohn E. Carlson
John E. Carlson
CMConsuelo M. De Moraes
Consuelo M. De Moraes
MMMark C. Mescher
Mark C. Mescher
JSJack C. Schultz
Jack C. Schultz

28 February 2018 in Metabolites
Verified
Journal Article
Open access
PDF file
MMMam Mboge
Mam Mboge
BMBrian Mahon
Brian Mahon
RMRobert Mckenna
Robert Mckenna
SFSusan Frost
Susan Frost
The pH of the tumor microenvironment drives the metastatic phenotype and chemotherapeutic resistance of tumors. Understanding the mechanisms underlying this pH-dependent phenomenon will lead to improved drug delivery and allow the identification of new therapeutic targets. This includes an understanding of the role pH plays in primary tumor cells, and the regulatory factors that permit cancer cells to thrive. Over the last decade, carbonic anhydrases (CAs) have been shown to be important mediators of tumor cell pH by modulating the bicarbonate and proton concentrations for cell survival and proliferation. This has prompted an effort to inhibit specific CA isoforms, as an anti-cancer therapeutic strategy. Of the 12 active CA isoforms, two, CA IX and XII, have been considered anti-cancer targets. However, other CA isoforms also show similar activity and tissue distribution in cancers and have not been considered as therapeutic targets for cancer treatment. In this review, we consider all the CA isoforms and their possible role in tumors and their potential as targets for cancer therapy.

15 October 2008 in New Phytologist
Verified
Journal Article
Open access
PDF file
SFSusan Frost
Susan Frost
MMMark C. Mescher
Mark C. Mescher
CDChristopher Dervinis
Christopher Dervinis
John DavisJohn Davis
John Davis
JCJohn E. Carlson
John E. Carlson
CMConsuelo M. De Moraes
Consuelo M. De Moraes
• Herbivore-induced plant volatiles (HIPVs), in addition to attracting natural enemies of herbivores, can serve a signaling function within plants to induce or prime defenses. However, it is largely unknown, particularly in woody plants, which volatile compounds within HIPV blends can act as signaling molecules. • Leaves of hybrid poplar saplings were exposed in vivo to naturally wound-emitted concentrations of the green leaf volatile (GLV) cis-3-hexenyl acetate (z3HAC) and then subsequently fed upon by gypsy moth larvae. Volatiles were collected throughout the experiments, and leaf tissue was collected to measure phytohormone concentrations and expression of defense-related genes. • Relative to controls, z3HAC-exposed leaves had higher concentrations of jasmonic acid and linolenic acid following gypsy moth feeding. Furthermore, z3HAC primed transcripts of genes that mediate oxylipin signaling and direct defenses, as determined by both qRT-PCR and microarray analysis using the AspenDB 7 K expressed sequence tags (EST) microarray containing c. 5400 unique gene models. Moreover, z3HAC primed the release of terpene volatiles. • The widespread priming response suggests an adaptive benefit to detecting z3HAC as a wound signal. Thus, woody plants can detect and use z3HAC as a signal to prime defenses before actually experiencing damage. GLVs may therefore have important ecological functions in arboreal ecosystems.

18 March 2022 in Science
Verified
Journal Article
Closed access
JSJames S. Santangelo
James S. Santangelo
RNRob W. Ness
Rob W. Ness
BCBeata Cohan
Beata Cohan
CFConnor R. Fitzpatrick
Connor R. Fitzpatrick
SISimon G. Innes
Simon G. Innes
MJMarc T. J. Johnson
Marc T. J. Johnson
Urbanization transforms environments in ways that alter biological evolution. We examined whether urban environmental change drives parallel evolution by sampling 110,019 white clover plants from 6169 populations in 160 cities globally. Plants were assayed for a Mendelian antiherbivore defense that also affects tolerance to abiotic stressors. Urban-rural gradients were associated with the evolution of clines in defense in 47% of cities throughout the world. Variation in the strength of clines was explained by environmental changes in drought stress and vegetation cover that varied among cities. Sequencing 2074 genomes from 26 cities revealed that the evolution of urban-rural clines was best explained by adaptive evolution, but the degree of parallel adaptation varied among cities. Our results demonstrate that urbanization leads to adaptation at a global scale.