Prostate Development

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Historic drawing of the fetal male urogenital system

In humans, the male accessory glands are the seminal vesicles, prostate gland, and the bulbourethral glands. The male gonad, the testis, differentiates embryonically initially under the influence of the Y chromosome. Later under the influence the gonad-derived fetal testosterone acting through androgen receptors, a region of the urogenital sinus (UGS) mesenchyme differentiates to form the primordial prostate buds. The buds then signal back to the overlying epithelium, inducing duct formation, this was one of the early studied (1970's) example of an mesenchymal-epithelial interaction in development. Interestingly, the female equivalent gland originally called Skene's gland, then paraurethral gland has now also been renamed the female prostate.

The reproductive function of the prostate becomes active at puberty where prostate secretions contribute the majority by volume of the ejaculate containing spermatozoa.

The prostate gland is generally in the news due to its late postnatal adult growth changes, enlarged due to benign nodular hyperplasia, and the male health effects of prostate cancer. Prostate cancer is the second most common malignant tumor in western males and anatomically involves the prostate peripheral zone.

There are also currently separate pages describing Genital - Male Development | Spermatozoa Development | Testis Development | Prostate Development | Category:Prostate

Genital Links: Introduction | Lecture - Medicine | Lecture - Science | Lecture Movie | Medicine - Practical | Primordial Germ Cell | Meiosis | Female | Ovary | Oocyte | Uterus | Vagina | Reproductive Cycles | Menstrual Cycle | Male | Testis | Spermatozoa | Penis | Prostate | Genital Movies | Abnormalities | Assisted Reproductive Technology | Puberty | Category:Genital
Historic Embryology - Genital 
1902 The Uro-Genital System | 1904 Ovary and Testis | 1904 Leydig Cells | 1904 Hymen | 1905 Testis vascular | 1909 Prostate | 1912 Prostate | 1912 Urinogenital Organ Development | 1914 Female | 1915 Cowper’s and Bartholin’s Glands | 1920 Wolffian tubules | 1921 Urogenital Development | 1921 External Genital | 1927 Female Foetus 15 cm | 1932 Postnatal Ovary | 1935 Prepuce | 1935 Wolffian Duct | 1942 Sex Cords | 1943 Testes Descent | 1953 Germ Cells | Historic Embryology Papers | Historic Disclaimer

Lowsley OS. The development of the human prostate gland with reference to the development of other structures at the neck of the urinary bladder. (1912) Amer. J Anat. 13(3): 299-346.

Some Recent Findings

Male urogenital development (stage 22)
  • Contribution of Caudal Müllerian Duct Mesenchyme to Prostate Development[1] "It is unclear, however, how the urogenital sinus epithelium can derive both adult urethral glands and prostate epithelia. ...In this study we demonstrate that the caudal Müllerian duct mesenchyme (CMDM) drives prostate epithelial differentiation and is a key determinant in cell lineage specification between urethral glands and prostate epithelia. Utilizing both human embryonic stem cells and mouse embryonic tissues, we document that the CMDM is capable of inducing the specification of androgen receptor, prostate-specific antigen, NKX3.1, and Hoxb13-positive prostate epithelial cells."
  • Differential gene expression profiling of functionally and developmentally distinct human prostate epithelial populations[2] "Human fetal prostate buds appear in the 10th gestational week as solid cords, which branch and form lumens in response to androgen 1. Previous in vivo analysis of prostate epithelia isolated from benign prostatectomy specimens indicated that Epcam⁺ CD44⁻ CD49f(Hi) basal cells possess efficient tubule initiation capability relative to other subpopulations 2. Stromal interactions and branching morphogenesis displayed by adult tubule-initiating cells (TIC) are reminiscent of fetal prostate development. In the current study, we evaluated in vivo tubule initiation by human fetal prostate cells and determined expression profiles of fetal and adult epithelial subpopulations in an effort to identify pathways used by TIC."
  • The role of Wnt5a in prostate gland development[3] "The Wnt genes encode a large family of secreted glycoproteins that play important roles in controlling tissue patterning, cell fate and proliferation during development. Currently, little is known regarding the role(s) of Wnt genes during prostate gland development. The present study examines the role of the noncanonical Wnt5a during prostate gland development in rat and murine models. In the rat prostate, Wnt5a mRNA is expressed by distal mesenchyme during the budding stage and localizes to periductal mesenchymal cells with an increasing proximal-to-distal gradient during branching morphogenesis. Wnt5a protein is secreted and localizes to periductal stroma, extracellular matrix and epithelial cells in the distal ducts. While Wnt5a expression is high during active morphogenesis in all prostate lobes, ventral prostate (VP) expression declines rapidly following morphogenesis while dorsal (DP) and lateral lobe (LP) expression remains high into adulthood. Steroids modulate prostatic Wnt5a expression during early development with testosterone suppressing Wnt5a and neonatal estrogen increasing expression."
More recent papers  
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Search term: Prostate Embryology

Natalia Glatzel-Plucinska, Aleksandra Piotrowska, Jedrzej Grzegrzolka, Mateusz Olbromski, Adam Rzechonek, Piotr Dziegiel, Marzenna Podhorska-Okolow SATB1 Level Correlates with Ki-67 Expression and Is a Positive Prognostic Factor in Non-small Cell Lung Carcinoma. Anticancer Res.: 2018, 38(2);723-736 PubMed 29374696

Weimin Fan, Yali Xu, Yue Liu, Zhengqing Zhang, Liming Lu, Zhide Ding Obesity or Overweight, a Chronic Inflammatory Status in Male Reproductive System, Leads to Mice and Human Subfertility. Front Physiol: 2017, 8;1117 PubMed 29354072

Amin El-Heliebi, Claudia Hille, Navya Laxman, Jessica Svedlund, Christoph Haudum, Erkan Ercan, Thomas Kroneis, Shukun Chen, Maria Smolle, Christopher Rossmann, Tomasz Krzywkowski, Annika Ahlford, Evangelia Darai, Gunhild von Amsberg, Winfried Alsdorf, Frank König, Matthias Löhr, Inge de Kruijff, Sabine Riethdorf, Tobias M Gorges, Klaus Pantel, Thomas Bauernhofer, Mats Nilsson, Peter Sedlmayr In Situ Detection and Quantification of AR-V7, AR-FL, PSA, and KRAS Point Mutations in Circulating Tumor Cells. Clin. Chem.: 2018; PubMed 29301749

H Rouhrazi, N Turgan, G Oktem Zoledronic acid overcomes chemoresistance by sensitizing cancer stem cells to apoptosis. Biotech Histochem: 2018;1-12 PubMed 29300112

Selahattin Çalışkan, Muzaffer Oğuz Keleş, Metin İshak Öztürk, Musab Ali Kutluhan, Olgu Enis Tok, Feriha Ercan, Muhammet İhsan Karaman Effect of sildenafil citrate in testosterone induced benign prostate hyperplasia rat model. Turk J Urol: 2017, 43(4);434-438 PubMed 29201504


Historic drawing of the human prostate
  • Human Embryology (2nd ed.) Larson Chapter 10 p261-306
  • The Developing Human: Clinically Oriented Embryology (6th ed.) Moore and Persaud Chapter 13 p303-346
  • Before We Are Born (5th ed.) Moore and Persaud Chapter 14 p289-326
  • Essentials of Human Embryology, Larson Chapter 10 p173-205
  • Human Embryology, Fitzgerald and Fitzgerald Chapter 21-22 p134-152
  • Developmental Biology (6th ed.) Gilbert Chapter 14 Intermediate Mesoderm

Prostate Development Overview

  1. fetal testosterone stimulates urogenital sinus mesenchyme through androgen receptors
  2. urogenital sinus mesenchyme acts on the overlying epithelium to stimulate cell proliferation
  3. urogenital sinus epithelium then forms prostate ductal progenitor, the prostatic buds
  4. prostatic buds then grow into the urogenital sinus mesenchyme

Prostate Bud Growth

  1. specification phase - instructive developmental cues define where buds will form in the UGS
  2. initiation phase - prostatic buds begin to form
  3. elongation phase - proliferation, cell adhesion, and cell migration coordinate outgrowth of prostatic buds into UGM.

Based on the recent review.[4]

Fetal Prostate

Data and images from a 1912 study by Lowsley.[5] (See all images)

Table showing number of tubules of each Prostate Lobe opening into prostatic urethra, the number of Albarran' s tubules, and the number of subtrigonal tubules.
Size of Fetus

Measurement (cm)

Total No. of
Prostatic Tubules
Glands of Albarran
7.5 12 39 11 12 74 0 0
8 7 27 6 13 53 0 0
12.5 10 46 4 14 74 8 0
19 0 42 10 7 59 11 5
27 11 36 9 8 64 9 4
36 9 34 11 2 56 19 9
Averages 10 37 8 9 63 12 6
The averages are taken from the specimens in which the structure is present in case of middle lobe and the groups of Albarran and the subtrigonal group.

Links: Fetal Development

Genital Development Overview

Three main stages during development, mesonephric/paramesonephric duct changes are one of the first male/female differences that occur in development, while external genitaila remain indeterminate in appearance for quite a while.

  1. Differentiation of gonad (Sex determination)
  2. Differentiation of internal genital organs
  3. Differentiation of external genital organs

The 2nd and 3rd stages dependent on endocrine gonad. Reproductive development has a long maturation timecourse, begining in the embryo and finishing in puberty. (More? Puberty Development)

Mouse Prostate Development

The mouse has been used extensively as a model of prostate embryonic development. A similar androgenic regulation occurs of in ventral epithelial bud affecting number and pattern forming in the mouse urogenital sinus.[6]

  • begins in fetal mice ductal progenitors (or buds) emerge from urogenital sinus epithelium
  • prostatic buds develop in response to androgens, which activate androgen receptors in UGS mesenchyme
  • two rows of 3-4 prostatic buds at birth

Links: Mouse Development

Prostate Histology

Prostate histology 01.jpg Prostate histology 02.jpg Prostate histology 03.jpg
Human prostate histology Corpora Amylacea Submucosal gland
(adult, (Stain - Haematoxylin Eosin) low power overview) (adult, (Stain - Haematoxylin Eosin) detail) (adult, (Stain - Haematoxylin Eosin) high power detail)


The prostate is the largest accessory sex gland in men (about 2 × 3 × 4 cm). It contains 30 - 50 tubuloalveolar glands, which empty into 15 - 25 independent excretory ducts. These ducts open into the urethra. The glands are embedded into a fibromuscular stroma, which mainly consists of smooth muscle separated by strands of connective tissue rich in collagenous and elastic fibres. The muscle forms a dense mass around the urethra and beneath the fairly thin capsule of the prostrate.

Macroscopically the prostrate can be divided into lobes, but they are inconspicuous in histological sections. In good histological sections it is possible to distinguish three concentric zones, which surround the prostatic part of the urethra.

  • peripheral zone contains large (main glands) whose ducts run posteriorly to open into the urethra
  • internal zone consists of the so-called submucosal glands
  • innermost zone contains mucosal glands

Secretory Glands

The secretory alveoli of the prostate are very irregularly shaped because of papillary projections of the mucosa into the lumen of the gland. The epithelium is cuboidal or columnar. Basal cells are again present, and the epithelium may look pseudostratified where they are found. The secretory cells are slightly acidophilic and secretory granules may be visible in the cytoplasm. Small extensions of the apical cytoplasm into the lumen of the alveoli may represent cells which release their secretory products (secretion is apocrine/merocine). The secretion of the prostate contains citric acid, the enzyme fibrinolysin (liquefies the semen), acid phosphatase, a number of other enzymes and lipids. The secretion of the prostate is the first fraction of the ejaculate.

The secretory ducts of the prostate are lined by a simple columnar epithelium, which changes to a transitional epithelium near the openings of the ducts into the urethra.

Corpora Amylacea

A characteristic feature of the prostate is the appearance of corpora amylacea in the secretory alveoli. They are rounded eosinophilic bodies. Their average diameter is about 0.25 mm (up to 2 mm). They appear already in the seventh month of foetal development. Their number increases with age - in particular past 50. They may undergo calcification. Corpora amylacea may appear in semen.

Additional Histology Images

Above text and images modified from: Blue Histology - Prostate


Genital development animations

Urogenital sinus 001 icon.jpg Urogenital septum 001 icon.jpg
Urogenital Sinus Urogenital Septum
Male external 001 icon.jpg Testis 001 icon.jpg
Male External Testis Descent

Historic Images of Genital Changes

Urogenital Indifferent Urogenital Male Urogenital Female
Urogenital indifferent Urogenital male Urogenital female

Historic Gray's Anatomy - The Prostate

Fig. 1160 – Prostate with seminal vesicles and seminal ducts, viewed from in front and above. (Spalteholz.)

(Prostata; Prostate Gland)

The prostate (Fig. 1160) is a firm, partly glandular and partly muscular body, which is placed immediately below the internal urethral orifice and around the commencement of the urethra. It is situated in the pelvic cavity, below the lower part of the symphysis pubis, above the superior fascia of the urogenital diaphragm, and in front of the rectum, through which it may be distinctly felt, especially when enlarged. It is about the size of a chestnut and somewhat conical in shape, and presents for examination a base, an apex, an anterior, a posterior and two lateral surfaces.

The base (basis prostatæ) is directed upward, and is applied to the inferior surface of the bladder, The greater part of this surface is directly continuous with the bladder wall; the urethra penetrates it nearer its anterior than its posterior border.

The apex (apex prostatæ) is directed downward, and is in contact with the superior fascia of the urogenital diaphragm.


The posterior surface (facies posterior) is flattened from side to side and slightly convex from above downward; it is separated from the rectum by its sheath and some loose connective tissue, and is distant about 4 cm. from the anus. Near its upper border there is a depression through which the two ejaculatory ducts enter the prostate. This depression serves to divide the posterior surface into a lower larger and an upper smaller part. The upper smaller part constitutes the middle lobe of the prostate and intervenes between the ejaculatory ducts and the urethra; it varies greatly in size, and in some cases is destitute of glandular tissue. The lower larger portion sometimes presents a shallow median furrow, which imperfectly separates it into a right and a left lateral lobe: these form the main mass of the gland and are directly continuous with each other behind the urethra. In front of the urethra they are connected by a band which is named the isthmus: this consists of the same tissues as the capsule and is devoid of glandular substance.

The anterior surface (facies anterior) measures about 2.5 cm. from above downward but is narrow and convex from side to side. It is placed about 2 cm. behind the pubic symphysis, from which it is separated by a plexus of veins and a quantity of loose fat. It is connected to the pubic bone on either side by the puboprostatic ligaments. The urethra emerges from this surface a little above and in front of the apex of the gland.

The lateral surfaces are prominent, and are covered by the anterior portions of the Levatores ani, which are, however, separated from the gland by a plexus of veins.

The prostate measures about 4 cm. transversely at the base, 2 cm. in its antero-posterior diameter, and 3 cm. in its vertical diameter. Its weight is about 8 gm. It is held in its position by the puboprostatic ligaments; by the superior fascia of the urogenital diaphragm, which invests the prostate and the commencement of the membranous portion of the urethra; and by the anterior portions of the Levatores ani, which pass backward from the pubis and embrace the sides of the prostate. These portions of the Levatores ani, from the support they afford to the prostate, are named the Levatores prostatæ.

The prostate is perforated by the urethra and the ejaculatory ducts. The urethra usually lies along the junction of its anterior with its middle third. The ejaculatory ducts pass obliquely downward and forward through the posterior part of the prostate, and open into the prostatic portion of the urethra.


The prostate is immediately enveloped by a thin but firm fibrous capsule, distinct from that derived from the fascia endopelvina, and separated from it by a plexus of veins. This capsule is firmly adherent to the prostate and is structurally continuous with the stroma of the gland, being composed of the same tissues, viz.: non-striped muscle and fibrous tissue. The substance of the prostate is of a pale reddish-gray color, of great density, and not easily torn. It consists of glandular substance and muscular tissue.

The muscular tissue according to Kölliker, constitutes the proper stroma of the prostate; the connective tissue being very scanty, and simply forming between the muscular fibers, thin trabeculæ, in which the vessels and nerves of the gland ramify. The muscular tissue is arranged as follows: immediately beneath the fibrous capsule is a dense layer, which forms an investing sheath for the gland; secondly, around the urethra, as it lies in the prostate, is another dense layer of circular fibers, continuous above with the internal layer of the muscular coat of the bladder, and blending below with the fibers surrounding the membranous portion of the urethra. Between these two layers strong bands of muscular tissue, which decussate freely, form meshes in which the glandular structure of the organ is imbedded. In that part of the gland which is situated in front of the urethra the muscular tissue is especially dense, and there is here little or no gland tissue; while in that part which is behind the urethra the muscular tissue presents a wide-meshed structure, which is densest at the base of the gland—that is, near the bladder—becoming looser and more sponge-like toward the apex of the organ.

The glandular substance is composed of numerous follicular pouches the lining of which frequently shows papillary elevations. The follicles open into elongated canals, which join to form from twelve to twenty small excretory ducts. They are connected together by areolar tissue, supported by prolongations from the fibrous capsule and muscular stroma, and enclosed in a delicate capillary plexus. The epithelium which lines the canals and the terminal vesicles is of the columnar variety. The prostatic ducts open into the floor of the prostatic portion of the urethra, and are lined by two layers of epithelium, the inner layer consisting of columnar and the outer of small cubical cells. Small colloid masses, known as amyloid bodies are often found in the gland tubes.

Vessels and Nerves

The arteries supplying the prostate are derived from the internal pudendal, inferior vesical, and middle hemorrhoidal. Its veins form a plexus around the sides and base of the gland; they receive in front the dorsal vein of the penis, and end in the hypogastric veins. The nerves are derived from the pelvic plexus.

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Gray H. Anatomy of the human body. (1918) Philadelphia: Lea & Febiger.

Cite this page: Hill, M.A. (2018, February 23) Embryology Prostate Development. Retrieved from

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Benign Nodular Hyperplasia

A postnatal adult ageing effect with an onset about 45 years of age, the prostate becomes enlarged due to benign nodular hyperplasia. By 60 years of age and older about 3/4 of the males are affected of which half will be symptomatic. This condition affects the mucosal glands.

Prostate Cancer

Prostate cancer is the second most common malignant tumor in western males and anatomically involves the prostate peripheral zone.

The dog has been used as a model of this condition as this species also spontaneously develop prostatic neoplasia. The cell line CT1258 has been derived from a spontaneous canine prostate carcinoma and can induce tumour formation in mice.

(More? "Movember")


  1. Hannah Brechka, Erin McAuley, Sophia M Lamperis, Gladell Paner, Donald Vander Griend Contribution of Caudal Müllerian Duct Mesenchyme to Prostate Development. Stem Cells Dev.: 2016; PubMed 27595922
  2. Haibo Liu, Radu M Cadaneanu, Kevin Lai, Baohui Zhang, Lihong Huo, Dong Sun An, Xinmin Li, Michael S Lewis, Isla P Garraway Differential gene expression profiling of functionally and developmentally distinct human prostate epithelial populations. Prostate: 2015, 75(7);764-76 PubMed 25663004
  3. Liwei Huang, Yongbing Pu, Wen Yang Hu, Lynn Birch, Douglas Luccio-Camelo, Terry Yamaguchi, Gail S Prins The role of Wnt5a in prostate gland development. Dev. Biol.: 2009, 328(2);188-99 PubMed 19389372
  4. Chad M Vezina, Tien-Min Lin, Richard E Peterson AHR signaling in prostate growth, morphogenesis, and disease. Biochem. Pharmacol.: 2009, 77(4);566-76 PubMed 18977204
  5. Lowsley OS. The development of the human prostate gland with reference to the development of other structures at the neck of the urinary bladder. (1912) Amer. J Anat. 13(3): 299-346.
  6. Sarah H Allgeier, Tien-Min Lin, Robert W Moore, Chad M Vezina, Lisa L Abler, Richard E Peterson Androgenic regulation of ventral epithelial bud number and pattern in mouse urogenital sinus. Dev. Dyn.: 2010, 239(2);373-85 PubMed 19941349

Pubmed Bookshelf


Joshua J Meeks, Edward M Schaeffer Genetic regulation of prostate development. J. Androl.: 2010, 32(3);210-7 PubMed 20930191

Yi Cai Participation of caudal müllerian mesenchyma in prostate development. J. Urol.: 2008, 180(5);1898-903 PubMed 18801537

Axel A Thomson Mesenchymal mechanisms in prostate organogenesis. Differentiation: 2008, 76(6);587-98 PubMed 18752494

Gerald R Cunha Mesenchymal-epithelial interactions: past, present, and future. Differentiation: 2008, 76(6);578-86 PubMed 18557761

Barry G Timms Prostate development: a historical perspective. Differentiation: 2008, 76(6);565-77 PubMed 18462432

Paul C Marker, Annemarie A Donjacour, Rajvir Dahiya, Gerald R Cunha Hormonal, cellular, and molecular control of prostatic development. Dev. Biol.: 2003, 253(2);165-74 PubMed 12645922

H G Kim, J Kassis, J C Souto, T Turner, A Wells EGF receptor signaling in prostate morphogenesis and tumorigenesis. Histol. Histopathol.: 1999, 14(4);1175-82 PubMed 10506934

G R Cunha, A A Donjacour Mesenchymal-epithelial interactions in the growth and development of the prostate. Cancer Treat. Res.: 1989, 46;159-75 PubMed 2577188


Sarah Hicks Allgeier, Chad M Vezina, Tien-Min Lin, Robert W Moore, Allen E Silverstone, Motoko Mukai, Jerrie Gavalchin, Paul S Cooke, Richard E Peterson Estrogen signaling is not required for prostatic bud patterning or for its disruption by 2,3,7,8-tetrachlorodibenzo-p-dioxin. Toxicol. Appl. Pharmacol.: 2009, 239(1);80-6 PubMed 19523480

Sarah Hicks Allgeier, Tien-Min Lin, Chad M Vezina, Robert W Moore, Wayne A Fritz, Shing-Yan Chiu, ChuanLi Zhang, Richard E Peterson WNT5A selectively inhibits mouse ventral prostate development. Dev. Biol.: 2008, 324(1);10-7 PubMed 18804104

Chad M Vezina, Sarah H Allgeier, Wayne A Fritz, Robert W Moore, Michael Strerath, Wade Bushman, Richard E Peterson Retinoic acid induces prostatic bud formation. Dev. Dyn.: 2008, 237(5);1321-33 PubMed 18393306

Hongyun Wang, Irwin Leav, Soichiro Ibaragi, Michael Wegner, Guo-fu Hu, Michael L Lu, Steven P Balk, Xin Yuan SOX9 is expressed in human fetal prostate epithelium and enhances prostate cancer invasion. Cancer Res.: 2008, 68(6);1625-30 PubMed 18339840

Crist Cook, Chad M Vezina, Sarah H Allgeier, Aubie Shaw, Min Yu, Richard E Peterson, Wade Bushman Noggin is required for normal lobe patterning and ductal budding in the mouse prostate. Dev. Biol.: 2007, 312(1);217-30 PubMed 18028901

Guy Letellier, Marie-José Perez, Mokrane Yacoub, Pierre Levillain, Olivier Cussenot, Gaëlle Fromont Epithelial phenotypes in the developing human prostate. J. Histochem. Cytochem.: 2007, 55(9);885-90 PubMed 17478449

G R Cunha, B Lung The possible influence of temporal factors in androgenic responsiveness of urogenital tissue recombinants from wild-type and androgen-insensitive (Tfm) mice. J. Exp. Zool.: 1978, 205(2);181-93 PubMed 681909


Evatt EJ. A contribution to the development of the prostate in man. (1909) Jour. of Anat. and Phys. 43: 314-321.

Lowsley OS. The development of the human prostate gland with reference to the development of other structures at the neck of the urinary bladder. (1912) Amer. J Anat. 13(3): 299-346.

Watson EM. The development of the seminal vesicles in man. (1918) Amer. J Anat. 24(4): 395 - 439.

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Search Pubmed "Prostate Embryology" Oct 2010 - All (775) Review (113) Free Full Text (171)

Search Pubmed: Prostate Embryology | Prostate Development | Corpora Amylacea |

Additional Images


Lowsley OS. The development of the human prostate gland with reference to the development of other structures at the neck of the urinary bladder. (1912) Amer. J Anat. 13(3): 299-346.


  • Albarran glands - (Albarran's glands, glands of Albarran) submucosal glands located in the subcervical region of the prostate gland that empty into the posterior urethra. Named after Joaquin Maria Albarrán y Dominguez (1860 – 1912) a Cuban urologist.
  • 5-α-reductase - enzyme that converts testosterone to dihydrotestosterone.
  • androgen receptor - (AR)
  • benign prostatic hyperplasia
  • mesenchyme - embryonic connective tissue
  • paraurethral gland - (Skene's gland) - female prostate gland is the correct nomenclature
  • prostate gland - Greek, prostates = "one who stands before", "protector", a female prostate gland exists
  • prostate cancer
  • UGE - urogenital epithelium
  • UGS - urogenital sinus
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Cite this page: Hill, M.A. (2018, February 23) Embryology Prostate Development. Retrieved from

What Links Here?
© Dr Mark Hill 2018, UNSW Embryology ISBN: 978 0 7334 2609 4 - UNSW CRICOS Provider Code No. 00098G