Evidence map›Paper›PMID 24225884›Full record

ReviewAmerican journal of physiology. Cell physiology2014

Cellular calcium dynamics in lactation and breast cancer: from physiology to pathology.

Brandie M Cross, Gerda E Breitwieser, Timothy A Reinhardt, Rajini Rao

Abstract readReview
In one paragraph

Review in American journal of physiology. Cell physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 10% 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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 85 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. iScience · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Altered SERCA Expression in Breast Cancer.Medicina (Kaunas, Lithuania) · 2021
    Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Calcium Metabolism and Breast Cancer: Echoes of Lactation?Current opinion in endocrine and metabolic research · 2020
    Article
  17. Breast Cancer and Microcalcifications: An Osteoimmunological Disorder?International journal of molecular sciences · 2020
    Review
  18. Primary Active CaCold Spring Harbor perspectives in biology · 2020
    Review
  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

4 authors at 3 institutions in 1 country.

Brandie M CrossDepartment of Physiology, The Johns Hopkins University, Baltimore, Maryland;
Gerda E Breitwieser
Timothy A Reinhardt
Rajini Rao
Johns Hopkins University · USGeisinger Medical Center · USNational Animal Disease Center · US

Funding

BIOCHEMISTRY, CELLULAR AND MOLECULAR BIOLOGY PROGRAMT32GM007445 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI GREEN, RACHEL · 1985 to 2021
$24.1M
SECRETORY PATHWAY CALCIUM AND MANGANESE PUMPSR01GM062142 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI RAO, RAJINI · 2001 to 2015
$3.6M
NIGMS NIH HHS GM-062142NIGMS NIH HHS R01 GM062142NIGMS NIH HHS T32 GM007445
6 · The paper itself

Abstract

Breast cancer is the second leading cause of cancer mortality in women, estimated at nearly 40,000 deaths and more than 230,000 new cases diagnosed in the U.S. this year alone. One of the defining characteristics of breast cancer is the radiographic presence of microcalcifications. These palpable mineral precipitates are commonly found in the breast after formation of a tumor. Since free Ca(2+) plays a crucial role as a second messenger inside cells, we hypothesize that these chelated precipitates may be a result of dysregulated Ca(2+) secretion associated with tumorigenesis. Transient and sustained elevations of intracellular Ca(2+) regulate cell proliferation, apoptosis and cell migration, and offer numerous therapeutic possibilities in controlling tumor growth and metastasis. During lactation, a developmentally determined program of gene expression controls the massive transcellular mobilization of Ca(2+) from the blood into milk by the coordinated action of calcium transporters, including pumps, channels, sensors and buffers, in a functional module that we term CALTRANS. Here we assess the evidence implicating genes that regulate free and buffered Ca(2+) in normal breast epithelium and cancer cells and discuss mechanisms that are likely to contribute to the pathological characteristics of breast cancer.

Indexed as

ApoptosisBreast NeoplasmsCalciumCalcium ChannelsCalcium SignalingCalcium-Transporting ATPasesCell MovementCell ProliferationFemaleGene Expression Regulation, NeoplasticHumansLactationReceptors, Calcium-SensingVascular CalcificationCalciumCalcium ChannelsCalcium-Transporting ATPasesCASR protein, humanReceptors, Calcium-Sensingbreast cancerlactationmammary epitheliumsecretory pathwaySPCA2

Identifiers

PMID24225884
PMCPMC3948975
OpenAlexW2004066403

What OpenQuestion holds

Textmetadata
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.