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== Hormones biosynthesis in adrenal cortex ==
== Hormones biosynthesis in adrenal cortex ==
* Cortisol is synthesized from cholesterol. Synthesis takes place in the zona fasciculata of the adrenal cortex.
* [[Cortisol]] is synthesized from [[cholesterol]]. Synthesis takes place in the [[zona fasciculata]] of the [[adrenal cortex]].
* Aldosterone is produced in the zona glomerulosa
* [[Aldosterone]] is produced in the [[zona glomerulosa]]
* Sex hormones are synthesized in in the zona reticularis
* [[Sex hormones]] are synthesized in in the [[zona reticularis]]
* The secretion of cortisol is controlled by hypothalamic-pituitary axis by the following mechanism:<sup>[[Cushing's syndrome pathophysiology#cite note-pmid26004339-1|[1]]][[Cushing's syndrome pathophysiology#cite note-pmid25480800-2|[2]]]</sup>
* The secretion of [[cortisol]] is controlled by [[Hypothalamic pituitary adrenal axis|hypothalamic-pituitary axis]] by the following mechanism:<sup>[[Cushing's syndrome pathophysiology#cite note-pmid26004339-1|[1]]][[Cushing's syndrome pathophysiology#cite note-pmid25480800-2|[2]]]</sup>
[[Paraventricular nucleus|Paraventricular nuclei]] in the [[hypothalamus]] release [[Corticotropin-releasing hormone|corticotropin releasing hormone]] (CRH).
[[Paraventricular nucleus|Paraventricular nuclei]] in the [[hypothalamus]] release [[Corticotropin-releasing hormone|corticotropin releasing hormone]] (CRH).



Revision as of 16:50, 25 September 2017

Adrenocortical carcinoma Microchapters

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Raviteja Guddeti, M.B.B.S. [2] Shivali Marketkar, M.B.B.S. [3] Ahmad Al Maradni, M.D. [4] Mohammed Abdelwahed M.D[5]

Overview

On gross pathology, a large tan-yellow surface with areas of hemorrhage and necrosis is a characteristic finding of adrenocortical carcinoma. On microscopic histopathological analysis, sheets of atypical cells with some resemblance to the cells of the normal adrenal cortex are a characteristic finding of adrenocortical carcinoma.

Pathophysiology

Spread can take several forms:[4]  

  • Direct invasion of the tumor capsule, invasion through the tumor capsule into extra-adrenal soft tissue
  • Direct invasion of lymphatic vessels in and around the capsule and nearby blood vessels. Metastatic deposits are largely similar to the primary tumor

ACCs can be graded into low- and high-grade carcinoma groups based on their mitotic rates ( >20 mitoses per 50 high-power fields vs. <20 mitoses per 50 high-power fields)

Mitotic rate was most closely associated with patient outcome.

ACCs in children behave in a more indolent fashion compared with the adult, that is why there are so many pediatric ACCs but few pediatric deaths.[5]

Genetics

The genetic dissection of ACC has revealed genomic aberrations that contribute to neoplastic transformation of adrenocortical cells:

1. Clonality

2. Gene expression arrays

  • Expression levels of BUB1B, PINK1, and DLG7 are identified in ACC.[12]

3. MicroRNAs

  • MicroRNAs are RNAs that are important in the regulation of gene expression.
  • Numerous miRNAs have been identified in the regulation of various cellular processes such as proliferation, apoptosis, and differentiation.[13]
  • Dysregulation of miRNAs, such as overexpression or deletion, plays an important role in diseases.
  • Mistargeting of the miRNAs, resulting in inhibition or activation of various oncogenes, tumor suppressors, and other factors important in tumor angiogenesis.[14]
  • The investigation identified 14 upregulated miRNAs and 9 downregulated miRNAs unique to ACC.[15]
  • Upregulated miRNAs in ACCs included miR-184, miR-210, and miR-503.
  • Downregulated miRNAs included miR-214, miR-375, and miR-511.[16]
  • Levels of miR-184, miR-503, and miR-511 are able to distinguish benign from malignant adrenal tumors.[16]
  • MiR-483 was found to be significantly upregulated in pediatric ACCs.
  • MiR-99a and miR-100 are bioinformatically predicted to target the 3- untranslated regions of IGF1R, RPTOR, and FRAP1 and were experimentally confirmed to target several components of the IGF-1 signaling pathway.[17]

4. Gene mutations

  • TP53 located on 17p13 is the most commonly mutated gene in ACC, present in at least one-third of ACCs.[19]
  • LOH in the gene encoding p16ink/ p14arf, CDKN2A is observed in a subset of ACCs. The tumor suppressor function of this gene has been established in multiple cancers. LOH of 11q13 has been identified in 83% of samples.[20]
  • MEN1 somatic mutations are unusual in sporadic ACC.[21]
  • The canonical Wnt pathway, the catenin gene, and CTNNB1 have been identified as activating point mutations in over 25% of both ACAs and ACCs in children and adults.[22]

5. Chromosomal aberrations

  • ACCs showed complex chromosomal alterations. ACCs contained multiple chromosomal gains or losses with a mean of 10 events.
  • The newest study confirmed increased alterations in ACC (44%) compared with ACAs (10%).
  • In ACCs, the frequently observed chromosomal gains at 5, 7, 12, 16, 19, and 20 and losses at 13 and 22 were confirmed.

6. Epigenetic changes

Cellular signaling pathway

1. IGF pathway

  • In the adult adrenal cortex, both IGF-1 and IGF-2 stimulate basal and ACTH-induced steroidogenesis.[25]
  • Overall, the main role of IGF-2 lies in fetal development and growth, whereas IGF-1 acts mainly postnatally.[26]
  • Prominent overexpression of IGF2 and alterations of the IGF2/H19 locus have been identified in sporadic ACC.[27]
  • The IGF2 gene is located on 11p15, which also includes a noncoding H19 gene and a cyclin-dependent kinase inhibitor, CDKN1C (p57KIP2) (216, 217), and 80% to 90% of all ACCs show very high IGF2 expression. Pediatric ACCs reveal a 20-fold overexpression of IGF2.[28][29]
  • Patients with high IGF2 expression levels and 11p15 LOH are associated with a 5-fold increased risk for recurrence and a shorter disease-free survival.[30]
  • loss of maternally expressed CDKN1C and H19, may contribute to adrenal tumorigenesis.[31]
  • The combination treatment of IGF-1R antagonists and mitotane resulted in a synergistic antiproliferative effect.[32]

2. WNT signaling pathway

  • The pathway is differentiated into 3 diverging signaling cascades dependent on signal conduction through:
  • Initial alterations of the WNT/ catenin system/pathway were identified in FAP.[34]
  • Inactivating mutations of AXIN2 (a component of the catenin destruction complex) have also been described in some adrenocortical tumors.[36]
  • Both nuclear catenin accumulation and activating CTNNB1 mutations are present in ACCs suggests that WNT activation is a part of ACA tumorigenesis.

3. Vascular endothelial growth factor

Hormones biosynthesis in adrenal cortex

Paraventricular nuclei in the hypothalamus release corticotropin releasing hormone (CRH).

CRH is transferred to anterior pituitary via the portal veins.

CRH stimulates the activity of corticotrophs; cells that produce proopiomelanocortin (POMC) in the anterior pituitary.

Corticotrophs produce adrenocorticotropic hormone (ACTH) by the post-translational modification of POMC.

ACTH is drained into systemic circulation via the pituitary capillaries and stimulates the adrenal cortex (zona fasciculata) to produce cortisol.

Cortisol acts on hypothalamus and pituitary through a feedback mechanism to regulate the secretion of CRH and ACTH.

source: By David Richfield (User:Slashme) and Mikael Häggström. Derived from previous version by Hoffmeier and Settersr.In external use, this diagram may be cited as:Häggström M, Richfield D (2014). "Diagram of the pathways of human steroidogenesis". Wikiversity Journal of Medicine 1 (1). DOI:10.15347/wjm/2014.005. ISSN 20018762. - Self-made using bkchem and inkscape, CC BY-SA 3.0, https://commons.wikimedia.org/w/index.php?curid=6355511

Associated Conditions

Associated diseases with adrenocortical carcinoma are:

Gross Pathology

  • On gross pathology, adrenocortical carcinomas are often large (>5 cm in largest diameter), with a tan-yellow cut surface and areas of hemorrhage and necrosis.
  • Their cut surface ranges from brown to orange to yellow depending on the lipid content of their cells. Necrosis is almost always present.
  • Typical ACC with a hypercellular population of cells with the earliest form of tumor necrosis.
  • A typical ACC with a solid growth pattern and abundant eosinophilic cytoplasm with focal clear areas, consistent with lipid.
A large adrenal cortical carcinoma resected from a 27-year-old woman. The tumor measured 17 cm in diameter and invaded kidney and spleen which necessitated en bloc removal of these organs with the tumor.

Shown above is a large adrenal cortical carcinoma resected from a 27-year-old woman. The tumor measured 17 cm in diameter and invaded kidney and spleen which necessitated en bloc removal of these organs with tumor. Patient had evidence of virilization.

Microscopic Pathology

On microscopic examination, the tumor usually displays sheets of atypical cells with some resemblance to the cells of the normal adrenal cortex. The presence of invasion and mitotic activity helps differentiate small cancers from adrenocortical adenomas.[42]

The Weiss criteria is the most reliable histopathological scoring system differentiating ACC from adrenocortical adenoma.

ACC can be diagnosed by the presence of at least 3 of the 9 Weiss criteria:

  • Nuclear grade III or IV
  • More than 5 mitotic figures/50 HPF, counting 10 random fields in area of greatest number of mitotic figures on 5 slides with the greatest number of mitosis
  • Presence of atypical mitotic figures (abnormal distribution of chromosomes or excessive number of mitotic spindles)
  • Clear or vacuolated cells comprising 25% or less of tumor
  • Diffuse architecture (more than 1/3 of tumor forms patternless sheets of cells; trabecular, cord, columnar, alveolar or nesting pattern is not considered to be diffuse)
  • Microscopic necrosis
  • Venous invasion (veins must have smooth muscles in wall; tumor cell clusters or sheets forming polypoid projections into vessel lumen or polypoid tumor thrombi covered by endothelial layer)
  • Sinusoidal invasion (sinusoid is endothelial lined vessel in adrenal gland with little supportive tissue; consider only sinusoids within tumor)
  • Capsular invasion (nests or cords of tumor extending into or through capsule with a stromal reaction); either incomplete or complete

Modified Weiss criteria (score of 3 or more suggests malignancy):

Micrograph of an adrenocortical carcinoma (left of image - dark blue) and the adrenal cortex it arose from (right-top of image - pink/light blue). Benign adrenal medulla is present (right-middle of image - gray/blue). H&E stain.

Video

Shown below is a video explaining the histology of adrenocortical carcinoma

{{#ev:youtube|7jMFENhPaOM}}

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