Evidence map›Paper›PMID 36543131›Full record

ArticleCell reports2022

A molecular atlas of the human postmenopausal fallopian tube and ovary from single-cell RNA and ATAC sequencing.

Ernst Lengyel, Yan Li, Melanie Weigert, Lisha Zhu, Heather Eckart, Melissa Javellana, Sarah Ackroyd, Jason Xiao, Susan Olalekan, Dianne Glass and 6 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
4.8field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

44 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 1 institution in 1 country.

Ernst LengyelSection of Gynecologic Oncology, Department of Obstetrics and Gynecology, The University of Chicago, Chicago, IL 60637, USA. Electronic address: elengyel@uchicago.edu.
Yan LiCenter for Research Informatics, The University of Chicago, Chicago, IL 60637, USA.
Melanie WeigertSection of Gynecologic Oncology, Department of Obstetrics and Gynecology, The University of Chicago, Chicago, IL 60637, USA.
Lisha ZhuCenter for Research Informatics, The University of Chicago, Chicago, IL 60637, USA.
Heather EckartSection of Genetic Medicine, Department of Medicine, The University of Chicago, Chicago, IL 60637, USA.
Melissa JavellanaSection of Gynecologic Oncology, Department of Obstetrics and Gynecology, The University of Chicago, Chicago, IL 60637, USA.
Sarah AckroydSection of Gynecologic Oncology, Department of Obstetrics and Gynecology, The University of Chicago, Chicago, IL 60637, USA.
Jason XiaoSection of Gynecologic Oncology, Department of Obstetrics and Gynecology, The University of Chicago, Chicago, IL 60637, USA.
Susan OlalekanSection of Genetic Medicine, Department of Medicine, The University of Chicago, Chicago, IL 60637, USA.
Dianne GlassSection of Gynecologic Oncology, Department of Obstetrics and Gynecology, The University of Chicago, Chicago, IL 60637, USA.
Shilpa IyerSection of Gynecologic Oncology, Department of Obstetrics and Gynecology, The University of Chicago, Chicago, IL 60637, USA.
Rahul KrishnanSection of Gynecologic Oncology, Department of Obstetrics and Gynecology, The University of Chicago, Chicago, IL 60637, USA.
Agnes Julia BileczDepartment of Pathology, The University of Chicago, Chicago, IL 60637, USA.
Ricardo LastraDepartment of Pathology, The University of Chicago, Chicago, IL 60637, USA.
Mengjie ChenSection of Genetic Medicine, Department of Medicine, The University of Chicago, Chicago, IL 60637, USA. Electronic address: mengjiechen@uchicago.edu.
Anindita BasuSection of Genetic Medicine, Department of Medicine, The University of Chicago, Chicago, IL 60637, USA. Electronic address: onibasu@uchicago.edu.
University of Chicago · US

Funding

Metabolic reprogramming of the tumor microenvironment and therapy resistanceR35CA264619 · NCI · UNIVERSITY OF CHICAGO · PI Ernst Lengyel · 2021 to 2026
$5.2M
New directions in single cell genomics method developmentR01GM126553 · NIGMS · UNIVERSITY OF CHICAGO · PI Mengjie Chen · 2017 to 2026
$2.9M
Profiling Transcriptional Heterogeneity in Microbial Cells at Single Cell resolution and High-throughput using Droplet MicrofluidicsDP2AI158157 · NIAID · UNIVERSITY OF CHICAGO · PI BASU, ANINDITA · 2020 to 2020
$2.4M
Nicotinamide N-Methyltransferase (NNMT) as a master regulator of cancer stromaR01CA211916 · NCI · UNIVERSITY OF CHICAGO · PI LENGYEL, ERNST · 2017 to 2021
$1.9M
Develop new bioinformatics infrastructures and computational tools for epitranscriptomics dataR01HG012927 · NHGRI · UNIVERSITY OF CHICAGO · PI Mengjie Chen · 2023 to 2026
$1.6M
Developing new computational tools for spatial transcriptomics dataR01HG011883 · NHGRI · UNIVERSITY OF CHICAGO · PI CHEN, MENGJIE, ZHOU, XIANG · 2021 to 2024
$1.5M
Functional contributions of glycogen metabolism to ovarian cancer metastasisR01CA237029 · NCI · UNIVERSITY OF CHICAGO · PI LENGYEL, ERNST · 2020 to 2021
$881k
NCI NIH HHS R01 CA211916NCI NIH HHS R01 CA237029NCI NIH HHS R35 CA264619NHGRI NIH HHS R01 HG011883NHGRI NIH HHS R01 HG012927NIAID NIH HHS DP2 AI158157NIGMS NIH HHS R01 GM126553
6 · The paper itself

Abstract

As part of the Human Cell Atlas Initiative, our goal is to generate single-cell transcriptomics (single-cell RNA sequencing [scRNA-seq], 86,708 cells) and regulatory (single-cell assay on transposase accessible chromatin sequencing [scATAC-seq], 59,830 cells) profiles of the normal postmenopausal ovary and fallopian tube (FT). The FT contains 11 major cell types, and the ovary contains 6. The dominating cell type in the FT and ovary is the stromal cell, which expresses aging-associated genes. FT epithelial cells express multiple ovarian cancer risk-associated genes (CCDC170, RND3, TACC2, STK33, and ADGB) and show active communication between fimbrial epithelial cells and ovarian stromal cells. Integrated single-cell transcriptomics and chromatin accessibility data show that the regulatory landscape of the fimbriae is different from other anatomic regions. Cell types with similar gene expression in the FT display transcriptional profiles. These findings allow us to disentangle the cellular makeup of the postmenopausal FT and ovary, advancing our knowledge of gynecologic diseases in menopause.

Indexed as

Fallopian TubesOvaryChromatinFemaleHumansPostmenopauseProtein Serine-Threonine KinasesRNASingle-Cell AnalysisChromatinProtein Serine-Threonine KinasesRNASTK33 protein, humancarcinomaCP: Cell biologyCP: Molecular biologyendometriosisfallopian tubesfemaleovarian epithelialovarian neoplasmsovarypost-menopausereproductive healthscATA-seqscRNA-seqsingle-cell analysis

Identifiers

PMID36543131
PMCPMC11295111
OpenAlexW4312084913

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.