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Cervix Uteri

Anatomy and Physiology · NLM MeSH · updated 2026-10-31 · version 1

Citations verified against PubMedNot yet clinician-reviewed10 referencesApproximately 4 min read

The neck portion of the uterus between the lower isthmus and the vagina forming the cervical canal.

Table of Contents

1. Definition2. Research landscape3. Reading the evidence4. Open-access studies5. Key reviews6. References7. About this article

Definition and research guide

This page combines a MeSH definition, publication statistics and selected research abstracts. It is a starting point for reading the literature, not a medical textbook or a systematic evidence review.

Content available: 4 complete abstracts (874 words), 10 references. Full article text is not stored or reproduced here; follow the PMID, DOI or PMC links to read the original sources and their access terms.

Definition

The neck portion of the uterus between the lower isthmus and the vagina forming the cervical canal.

Definition: NLM Medical Subject Headings (MeSH) scope note (Public domain (U.S. National Library of Medicine); attribution requested). View the MeSH record.

Also known as: Cervix; Cervixes; Uterine Cervix; Cervix, Uterine; Uterine Cervical Canal; Canal, Uterine Cervical; Uterine Cervical Canals; Cervical Canal of the Uterus.

Where it fits in the MeSH classification

Broader topics
Uterus
See also
Colposcopy

Related concepts

  • Uterus
  • Vagina

Research landscape

PubMed indexes 30,766 records tagged with the MeSH heading “Cervix Uteri” (counts retrieved 2026-10-31). 3,369 of them (11.0%) were published from 2020 onward, and the busiest period so far is through 1999 with 16,900 records.

Reviews account for 1,903 records (6.2%) and meta-analyses for 207. Randomized controlled trials number 989 (3.2%) as a share of all records on the topic.

PubMed records by publication periodthrough 1999: 16,900 records; 2000-2009: 4,759 records; 2010-2019: 5,738 records; 2020 onward: 3,369 records16,900through 19994,7592000-20095,7382010-20193,3692020 onward
Records in PubMed indexed with this heading, by publication period. Real counts from NCBI E-utilities; the final period covers only part of the current year. Volume reflects how much has been published, not how strong the evidence is.
Show the data
PeriodRecords
through 199916,900
2000-20094,759
2010-20195,738
2020 onward3,369
Share of records by publication typeReviews: 6.2 percent; Meta-analyses: 0.7 percent; Randomized controlled trials: 3.2 percentReviews6.2% (1,903)Meta-analyses0.7% (207)Randomized controlled trials3.2% (989)
Share of all PubMed records on this heading that carry each publication type. Types overlap with other records, so the shares do not sum to 100%.
Publication-type chart data
Publication types among 30,766 PubMed records
TypeRecordsShare
Reviews1,9036.2%
Meta-analyses2070.7%
Randomized controlled trials9893.2%

Method: PubMed query "Cervix Uteri"[MeSH Terms] with publication-type and date filters, retrieved 2026-10-31.

Reading the evidence in anatomy and physiology

Anatomy describes how body structures are built and physiology describes how they normally work, so most findings here are descriptive or mechanistic rather than evidence about treatment. Much of what is known comes from dissection, imaging, tissue studies and experiments in animals, and measurements in healthy volunteers can differ from those in people with disease or at different ages. Normal ranges vary between individuals and populations. Check whether a result was measured in people or in another species, the age and health of the participants, and the method used.

Evidence from open-access studies

These open-access studies come from PubMed’s best-match results for this heading (papers whose main topic it is), ranked here by citation count, with one recent addition. Each abstract is reproduced in full under its recorded open licence so that you can read the authors’ own words. They illustrate the literature; they are not a systematic summary of it. Citation counts measure attention, not reliability or clinical benefit.

Study comparison — selected abstracts, not a systematic review
Study / authorsYearSource label / designEurope PMC citationsLicence / source
Mucus production, host-microbiome interactions, hormone sensitivity, and innate immune responses modeled in human cervix chips
Izadifar Z, Cotton J, Chen S, Horvath V, Stejskalova A, Gulati A, et al.
2024Research article
Design not recorded in structured metadata
53cc by
PMID 38811586 · DOI · PMC11137093
Immunometabolic and potential tumor-promoting changes in 3D cervical cell models infected with bacterial vaginosis-associated bacteria
Maarsingh JD, Łaniewski P, Herbst-Kralovetz MM
2022Research article
Design not recorded in structured metadata
32cc by
PMID 35869172 · DOI · PMC9307755
The cervical microbiota of Hispanics living in Puerto Rico is nonoptimal regardless of HPV status
Vargas-Robles D, Romaguera J, Alvarado-Velez I, Tosado-Rodríguez E, Dominicci-Maura A, Sanchez M, et al.
2023Research article
Design not recorded in structured metadata
25cc by
PMID 37534938 · DOI · PMC10469956
The anterior cervical angle: A novel predictor of vaginal birth
Şeker E, Ümit C, Süt H, Koçar M, Sarıtaş E, Yıldız GA
2026Research article
Design not recorded in structured metadata
2cc by
PMID 40704678 · DOI · PMC12724038

Mucus production, host-microbiome interactions, hormone sensitivity, and innate immune responses modeled in human cervix chips [1]

Research article Izadifar Z, Cotton J, Chen S, Horvath V, Stejskalova A, Gulati A, et al. · · 2024 · cited 53 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
Modulation of the cervix by steroid hormones and commensal microbiome play a central role in the health of the female reproductive tract.
Closing excerpt
Thus, human Cervix Organ Chips represent physiologically relevant in vitro models to study cervix physiology and host-microbiome interactions, and hence may be used as a preclinical testbed for development of therapeutic interventions to enhance women's health.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (135 words)

Modulation of the cervix by steroid hormones and commensal microbiome play a central role in the health of the female reproductive tract. Here we describe organ-on-a-chip (Organ Chip) models that recreate the human cervical epithelial-stromal interface with a functional epithelial barrier and production of mucus with biochemical and hormone-responsive properties similar to living cervix. When Cervix Chips are populated with optimal healthy versus dysbiotic microbial communities (dominated by Lactobacillus crispatus and Gardnerella vaginalis, respectively), significant differences in tissue innate immune responses, barrier function, cell viability, proteome, and mucus composition are observed that are similar to those seen in vivo. Thus, human Cervix Organ Chips represent physiologically relevant in vitro models to study cervix physiology and host-microbiome interactions, and hence may be used as a preclinical testbed for development of therapeutic interventions to enhance women's health.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 38811586 · DOI · PMC11137093

Immunometabolic and potential tumor-promoting changes in 3D cervical cell models infected with bacterial vaginosis-associated bacteria [2]

Research article Maarsingh JD, Łaniewski P, Herbst-Kralovetz MM · · 2022 · cited 32 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
Specific bacteria of the human microbiome influence carcinogenesis at diverse anatomical sites.
Closing excerpt
This study provides mechanistic insights into how gynecologic cancer-associated bacteria might facilitate a tumor-promoting microenvironment in the human cervix.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (150 words)

Specific bacteria of the human microbiome influence carcinogenesis at diverse anatomical sites. Bacterial vaginosis (BV) is the most common vaginal disorder in premenopausal women that is associated with gynecologic sequelae, including cervical cancer. BV-associated microorganisms, such as Fusobacterium, Lancefieldella, Peptoniphilus, and Porphyromonas have been associated with gynecologic and other cancers, though the pro-oncogenic mechanisms employed by these bacteria are poorly understood. Here, we integrated a multi-omics approach with our three-dimensional (3-D) cervical epithelial cell culture model to investigate how understudied BV-associated bacteria linked to gynecologic neoplasia influence hallmarks of cancer in vitro. Lancefieldella parvulum and Peptoniphilus lacrimalis elicited robust proinflammatory responses in 3-D cervical cells. Fusobacterium nucleatum and Fusobacterium gonidiaformans modulated metabolic hallmarks of cancer corresponding to accumulation of 2-hydroxyglutarate, pro-inflammatory lipids, and signs of oxidative stress and genotoxic hydrogen sulfide. This study provides mechanistic insights into how gynecologic cancer-associated bacteria might facilitate a tumor-promoting microenvironment in the human cervix.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 35869172 · DOI · PMC9307755

The cervical microbiota of Hispanics living in Puerto Rico is nonoptimal regardless of HPV status [3]

Research article Vargas-Robles D, Romaguera J, Alvarado-Velez I, Tosado-Rodríguez E, Dominicci-Maura A, Sanchez M, et al. · · 2023 · cited 25 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
The cervicovaginal microbiota is influenced by host physiology, immunology, lifestyle, and ethnicity.
Closing excerpt
We believe this is a relevant and timely article expanding knowledge on the cervicovaginal microbiome of PR women, where we postulate that these highly diverse communities are conducive to cervical disease.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (372 words)

The cervicovaginal microbiota is influenced by host physiology, immunology, lifestyle, and ethnicity. We hypothesized that there would be differences in the cervicovaginal microbiota among pregnant, nonpregnant, and menopausal women living in Puerto Rico (PR) with and without human papillomavirus (HPV) infection and cervical cancer. We specifically wanted to determine if the microbiota is associated with variations in cervical cytology. A total of 294 women, including reproductive-age nonpregnant (N = 196), pregnant (N = 37), and menopausal (N = 61) women, were enrolled. The cervicovaginal bacteria were characterized by 16S rRNA amplicon sequencing, the HPV was genotyped with SPF10-LiPA, and cervical cytology was quantified. High-risk HPV (HR-HPV, 67.3%) was prevalent, including genotypes not covered by the 9vt HPV vaccine. Cervical lesions (34%) were also common. The cervical microbiota was dominated by Lactobacillus iners. Pregnant women in the second and third trimesters exhibited a decrease in diversity and abundance of microbes associated with bacterial vaginosis. Women in menopause had greater alpha diversity, a greater proportion of facultative and strictly anaerobic bacteria, and higher cervicovaginal pH than premenopausal women. Cervical lesions were associated with greater alpha diversity. However, no significant associations between the microbiota and HPV infection (HR or LR-HPV types) were found. The cervicovaginal microbiota of women living in Puerto Rican were either dominated by L. iners or diverse microbial communities regardless of a woman's physiological stage. We postulate that the microbiota and the high prevalence of HR-HPV increase the risk of cervical lesions among women living in PR. IMPORTANCE In the enclosed manuscript, we provide the first in-depth characterization of the cervicovaginal microbiota of Hispanic women living in Puerto Rico (PR), using a 16S rRNA approach, and include women of different physiological stages. Surprisingly we found that high-risk HPV was ubiquitous with a prevalence of 67.3%, including types not covered by the 9vt HPV vaccine. We also found highly diverse microbial communities across women groups-with a reduction in pregnant women, but dominated by nonoptimal Lactobacillus iners. Additionally, we found vaginosis-associated bacteria as Dialister spp., Gardnerella spp., Clostridium, or Prevotella among most women. We believe this is a relevant and timely article expanding knowledge on the cervicovaginal microbiome of PR women, where we postulate that these highly diverse communities are conducive to cervical disease.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 37534938 · DOI · PMC10469956

The anterior cervical angle: A novel predictor of vaginal birth [4]

Research article Şeker E, Ümit C, Süt H, Koçar M, Sarıtaş E, Yıldız GA · · 2026 · cited 2 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
ObjectiveThis study investigates the role of anterior utero-cervical angle as a predictor of labor induction success, comparing outcomes between normal vaginal delivery and cesarean section groups.
Closing excerpt
Further prospective studies are needed to clarify its clinical utility.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (217 words)

ObjectiveThis study investigates the role of anterior utero-cervical angle as a predictor of labor induction success, comparing outcomes between normal vaginal delivery and cesarean section groups.MethodsA prospective cohort study was conducted on 55 patients undergoing labor induction (46 normal vaginal delivery, 9 cesarean section). Parameters such as maternal age, weight, height, body mass index (BMI; calculated as weight in kilograms divided by the square of height in meters), cervical length, anterior cervical angle (ACA), Bishop score, and levator ani measurements were analyzed. Statistical significance was assessed using Fisher exact test, independent sample test, Mann-Whitney U test, or χ2 test (P ResultsThe ACA was significantly different between normal vaginal delivery (108.02 ± 22.38°) and cesarean section (86.11 ± 26.09°) groups (P = 0.026). We determined an optimal ACA threshold of 96° for the prediction of failure of progression (sensitivity: 70%, specificity: 73%). Other significant differences included maternal weight (P = 0.0033), height (P = 0.0033), BMI (P = 0.0462), primiparity (P = 0.0161), and fetal gender (P = 0.0334). However, Bishop score, cervical length, and levator ani metrics showed no significant differences.ConclusionAlthough ACA differs significantly between vaginal delivery and cesarean section groups, its independent predictive value for induction success remains limited compared with factors like primiparity and BMI. Further prospective studies are needed to clarify its clinical utility.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 40704678 · DOI · PMC12724038

Key reviews and meta-analyses

The most cited review-type papers among PubMed’s best-match results for this heading, listed with bibliographic details only. Follow the links for the full text and access terms.

  • Research article Cervical human papillomavirus prevalence in 5 continents: meta-analysis of 1 million women with normal cytological findings [5]
    Bruni L, Diaz M, Castellsagué X, Ferrer E, Bosch FX, de Sanjosé S · J Infect Dis · 2010 · cited 1,094 times (Europe PMC)
  • Research article p16(INK4a) immunostaining in cytological and histological specimens from the uterine cervix: a systematic review and meta-analysis [6]
    Tsoumpou I, Arbyn M, Kyrgiou M, Wentzensen N, Koliopoulos G, Martin-Hirsch P, et al. · Cancer Treat Rev · 2009 · cited 201 times (Europe PMC)
  • Research article Cervicovaginal microbiota, women's health, and reproductive outcomes [7]
    Kroon SJ, Ravel J, Huston WM · Fertil Steril · 2018 · cited 172 times (Europe PMC)
  • Research article Bacterial vaginosis and the cervicovaginal immune response [8]
    Mitchell C, Marrazzo J · Am J Reprod Immunol · 2014 · cited 165 times (Europe PMC)
  • Research article Role of Lactobacilli and Lactoferrin in the Mucosal Cervicovaginal Defense [9]
    Valenti P, Rosa L, Capobianco D, Lepanto MS, Schiavi E, Cutone A, et al. · Front Immunol · 2018 · cited 141 times (Europe PMC)
  • Research article Relationships between mechanical properties and extracellular matrix constituents of the cervical stroma during pregnancy [10]
    House M, Kaplan DL, Socrate S · Semin Perinatol · 2009 · cited 135 times (Europe PMC)

References

  1. Izadifar Z, Cotton J, Chen S, Horvath V, Stejskalova A, Gulati A, et al.. Mucus production, host-microbiome interactions, hormone sensitivity, and innate immune responses modeled in human cervix chips. . 2024. PMID 38811586 · DOI · PMC11137093
  2. Maarsingh JD, Łaniewski P, Herbst-Kralovetz MM. Immunometabolic and potential tumor-promoting changes in 3D cervical cell models infected with bacterial vaginosis-associated bacteria. . 2022. PMID 35869172 · DOI · PMC9307755
  3. Vargas-Robles D, Romaguera J, Alvarado-Velez I, Tosado-Rodríguez E, Dominicci-Maura A, Sanchez M, et al.. The cervical microbiota of Hispanics living in Puerto Rico is nonoptimal regardless of HPV status. . 2023. PMID 37534938 · DOI · PMC10469956
  4. Şeker E, Ümit C, Süt H, Koçar M, Sarıtaş E, Yıldız GA. The anterior cervical angle: A novel predictor of vaginal birth. . 2026. PMID 40704678 · DOI · PMC12724038
  5. Bruni L, Diaz M, Castellsagué X, Ferrer E, Bosch FX, de Sanjosé S. Cervical human papillomavirus prevalence in 5 continents: meta-analysis of 1 million women with normal cytological findings. J Infect Dis. 2010. PMID 21067372 · DOI
  6. Tsoumpou I, Arbyn M, Kyrgiou M, Wentzensen N, Koliopoulos G, Martin-Hirsch P, et al.. p16(INK4a) immunostaining in cytological and histological specimens from the uterine cervix: a systematic review and meta-analysis. Cancer Treat Rev. 2009. PMID 19261387 · DOI · PMC2784486
  7. Kroon SJ, Ravel J, Huston WM. Cervicovaginal microbiota, women's health, and reproductive outcomes. Fertil Steril. 2018. PMID 30098679 · DOI
  8. Mitchell C, Marrazzo J. Bacterial vaginosis and the cervicovaginal immune response. Am J Reprod Immunol. 2014. PMID 24832618 · DOI · PMC4128638
  9. Valenti P, Rosa L, Capobianco D, Lepanto MS, Schiavi E, Cutone A, et al.. Role of Lactobacilli and Lactoferrin in the Mucosal Cervicovaginal Defense. Front Immunol. 2018. PMID 29545798 · DOI · PMC5837981
  10. House M, Kaplan DL, Socrate S. Relationships between mechanical properties and extracellular matrix constituents of the cervical stroma during pregnancy. Semin Perinatol. 2009. PMID 19796726 · DOI · PMC2774809

About this article

Sources
NLM Medical Subject Headings (definition, synonyms); NCBI PubMed (counts, identifiers); Europe PMC (open-access abstracts and citation counts).
Verification
Every reference was resolved against PubMed on 2026-10-31; title, year and DOI matched.
Review state
automated source verified; no human expert review has been recorded yet.
Version
1, last updated 2026-10-31.

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At a glance

30,766
PubMed records on this heading
11%
published since 2020
1,903
review articles
989
randomized trials
10
verified references below

Counts come from PubMed on 2026-10-31; they show how much has been written, not how strong the evidence is.

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