Literature DB >> 24013142

Classifying chemical mode of action using gene networks and machine learning: a case study with the herbicide linuron.

Anna Ornostay1, Andrew M Cowie, Matthew Hindle, Christopher J O Baker, Christopher J Martyniuk.   

Abstract

The herbicide linuron (LIN) is an endocrine disruptor with an anti-androgenic mode of action. The objectives of this study were to (1) improve knowledge of androgen and anti-androgen signaling in the teleostean ovary and to (2) assess the ability of gene networks and machine learning to classify LIN as an anti-androgen using transcriptomic data. Ovarian explants from vitellogenic fathead minnows (FHMs) were exposed to three concentrations of either 5α-dihydrotestosterone (DHT), flutamide (FLUT), or LIN for 12h. Ovaries exposed to DHT showed a significant increase in 17β-estradiol (E2) production while FLUT and LIN had no effect on E2. To improve understanding of androgen receptor signaling in the ovary, a reciprocal gene expression network was constructed for DHT and FLUT using pathway analysis and these data suggested that steroid metabolism, translation, and DNA replication are processes regulated through AR signaling in the ovary. Sub-network enrichment analysis revealed that FLUT and LIN shared more regulated gene networks in common compared to DHT. Using transcriptomic datasets from different fish species, machine learning algorithms classified LIN successfully with other anti-androgens. This study advances knowledge regarding molecular signaling cascades in the ovary that are responsive to androgens and anti-androgens and provides proof of concept that gene network analysis and machine learning can classify priority chemicals using experimental transcriptomic data collected from different fish species.
© 2013.

Entities:  

Keywords:  17-β estradiol; 17beta-trenbolone; 24-dehydrocholesterol reductase; 5α-dihydrotestosterone; AR; AXIN1; BCL2-like 1; BCL2L1; BMPR; C; CSNK1E; CTNNB1; CYP17A1; CYP1B1; DHCR24; DHT; DVL1; E(2); EDCs; ER; FABP1; FDX1; FGF8; FHM; FLUT; FN1; FOS; FOXO; FRAT1; FSHB; FZD; GH1; GO; GSEA; GSK3B; Gene Ontology; GnRH; HNF1 homeobox B; HNF1B; Herbicides; ID1; IFT88; IL16; INPP5D; JUN; LDLR; LEFTY2; LIN; LRP6; MMP9; MOA; MYC; Machine learning; NUCB2; Notch signaling; PCK2; PCR; PCSK2; POMC; Parameter of cost; RBM; Radial Basis Machine; SEMA3A; SHBG; SLC5A1; SNEA; SOCS3; STAT; SVM; Sub-network enrichment analysis; Support Vector Machine; TB; TFE3; TGFBR; TH; Vtg; Wnt-frizzled pathway; androgen receptor; axin 1; bone morphogenetic protein receptor; casein kinase 1, epsilon; catenin (cadherin-associated protein), beta 1, 88kDa; cytochrome P450, family 1, subfamily B, polypeptide 1; cytochrome P450, family 17, subfamily A, polypeptide 1; disheveled, dsh homolog 1 (Drosophila); endocrine disrupting compounds; estrogen receptor; fathead minnow; fatty acid binding protein 1, liver; ferredoxin 1; fibroblast growth factor 8 (androgen-induced); fibronectin 1; flutamide; follicle stimulating hormone, beta polypeptide; forkhead box O3; frequently rearranged in advanced T-cell lymphomas; frizzled receptor; gene set enrichment analysis; glycogen synthase kinase 3 beta; gonadotropin-releasing hormone receptor; growth hormone 1; inhibitor of DNA binding 1, dominant negative helix–loop–helix protein; inositol polyphosphate-5-phosphatase, 145kDa; interleukin 16 (lymphocyte chemoattractant factor); intraflagellar transport 88 homolog (Chlamydomonas); jun oncogene; left–right determination factor 2; linuron; low density lipoprotein receptor; low density lipoprotein receptor-related protein 6; matrix metallopeptidase 9 (gelatinase B,92kDa gelatinase,92kDa type IV collagenase); mode of action; nucleobindin 2; phosphoenolpyruvate carboxykinase 2 (mitochondrial); polymerase chain reaction; proopiomelanocortin; proprotein convertase subtilisin/kexin type 2; sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A; sex hormone-binding globulin; signal transducer and activator of transcription; solute carrier family 5 (sodium/glucose cotransporter), member 1; sub-network enrichment analysis; suppressor of cytokine signaling 3; transcription factor binding to IGHM enhancer 3; transforming growth factor, beta receptor 1; tyrosine hydroxylase; v-fos FBJ murine osteosarcoma viral oncogene homolog; v-myc myelocytomatosis viral oncogene homolog (avian); vitellogenin

Mesh:

Substances:

Year:  2013        PMID: 24013142     DOI: 10.1016/j.cbd.2013.08.001

Source DB:  PubMed          Journal:  Comp Biochem Physiol Part D Genomics Proteomics        ISSN: 1744-117X            Impact factor:   2.674


  5 in total

Review 1.  'Omics' and endocrine-disrupting chemicals - new paths forward.

Authors:  Carmen Messerlian; Rosie M Martinez; Russ Hauser; Andrea A Baccarelli
Journal:  Nat Rev Endocrinol       Date:  2017-07-14       Impact factor: 43.330

2.  FRAT1 expression regulates proliferation in colon cancer cells.

Authors:  Kongxi Zhu; Jianqiang Guo; Hongjuan Wang; Weihua Yu
Journal:  Oncol Lett       Date:  2016-10-19       Impact factor: 2.967

3.  An Experimental Approach to Study the Effects of Realistic Environmental Mixture of Linuron and Propamocarb on Zebrafish Synaptogenesis.

Authors:  Giulia Caioni; Carmine Merola; Monia Perugini; Michele d'Angelo; Anna Maria Cimini; Michele Amorena; Elisabetta Benedetti
Journal:  Int J Environ Res Public Health       Date:  2021-04-27       Impact factor: 3.390

4.  Towards Sustainable Environmental Quality: Priority Research Questions for the Australasian Region of Oceania.

Authors:  Sally Gaw; Andrew Harford; Vincent Pettigrove; Graham Sevicke-Jones; Therese Manning; James Ataria; Tom Cresswell; Katherine A Dafforn; Frederic Dl Leusch; Bradley Moggridge; Marcus Cameron; John Chapman; Gary Coates; Anne Colville; Claire Death; Kimberly Hageman; Kathryn Hassell; Molly Hoak; Jennifer Gadd; Dianne F Jolley; Ali Karami; Konstantinos Kotzakoulakis; Richard Lim; Nicole McRae; Leon Metzeling; Thomas Mooney; Jackie Myers; Andrew Pearson; Minna Saaristo; Dave Sharley; Julia Stuthe; Oliver Sutherland; Oliver Thomas; Louis Tremblay; Waitangi Wood; Alistair Ba Boxall; Murray A Rudd; Bryan W Brooks
Journal:  Integr Environ Assess Manag       Date:  2019-09-13       Impact factor: 2.992

5.  Multi-omics phenotyping of the gut-liver axis reveals metabolic perturbations from a low-dose pesticide mixture in rats.

Authors:  Robin Mesnage; Maxime Teixeira; Daniele Mandrioli; Laura Falcioni; Mariam Ibragim; Quinten Raymond Ducarmon; Romy Daniëlle Zwittink; Caroline Amiel; Jean-Michel Panoff; Emma Bourne; Emanuel Savage; Charles A Mein; Fiorella Belpoggi; Michael N Antoniou
Journal:  Commun Biol       Date:  2021-04-14
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.