Differential gene expression in patients with anal fistula reveals high levels of prolactin receptor
Abstract
Background/Aim. There are limited data examining variations in the local expression of inflammatory mediators in anal fistulas where it is anticipated that an improved understanding of the inflammatory milieu might lead to the potential therapeutic option of instillation therapy in complicated cases. The aim of the present study was to examine prolactin receptors (PRLR) as inflammatory markers and to correlate their expression with both the complexity of anal fistulas and the likelihood of fistula recurrence. Methods. Microarray was used to screen the differentially expressed gene profile of anal fistula using anal mucosa samples with hemorrhoids with age- and sex-matched patients as controls and then a prospective analysis of 65 patients was conducted with anal fistulas. PRLR immunohistochemistry was performed to define expression in simple, complex and recurrent anal fistula cases. The quantitative image comparison was performed combining staining intensity with cellular distribution in order to create high and low score PRLR immunohistochemical groupings. Results. A differential expression profile of 190 genes was found. PRLR expression was 2.91 times lower in anal fistula compared with control. Sixty-five patients were assessed (35 simple, 30 complex cases). Simple fistulas showed significantly higher PRLR expression than complex cases with recurrent fistulae showing overall lower PRLR expression than de novo cases (p = 0.001). These findings were reflected in measurable integrated optical density for complex and recurrent cases (complex cases, 8.31 ± 4.91 ´ 104 vs simple cases, 12.30 ± 6.91 ´ 104; p < 0.01; recurrent cases, 7.21 ± 3.51 ´ 104 vs primarily healing cases, 8.31 ± 4.91 ´ 104; p < 0.05). In univariate regression analysis, low PRLR expression correlated with fistula complexity; a significant independent effect maintained in multivariate analysis odds ratio [(OR) low to high PRLR expression = 9.52; p = 0.001)]. Conclusion. PRLR expression inversely correlates with anal fistula complexity. Further work must define the specificity of this finding and its relationship to other conventional mediators of inflammation.
References
Steele SR, Kumar R, Feingold DL, Rafferty JL, Buie WD. Standards Practice Task Force of the American Society of Colon and Rectal Surgeons. Practice parameters for the management of perianal abscess and fistula-in-ano. Dis Colon Rectum 2011; 54(12): 1465–74.
Kronborg O. To lay open or excise a fistula-in-ano: a rando-mized trial. Br J Surg 1985; 72(12): 970.
Alasari S, Kim NK. Overview of anal fistula and systematic
review of ligation of the intersphincteric fistula tract (LIFT). Tech Coloproctol 2014; 18(1): 13–22.
Lunniss PJ, Kamm MA, Phillips RK. Factors affecting continence after surgery for anal fistula. Br J Surg 1994; 81(9): 1382–5.
Garcia-Aguilar J, Belmonte C, Wong DW, Goldberg SM, Madoff RD. Anal fistula surgery. Factors associated with recurrence and in-continence. Dis Colon Rectum 1996;39(7): 723–9.
Sangwan YP, Rosen L, Riether RD, Stasik JJ, Sheets JA, Khubchan-dani IT. Is simple fistula-in-ano simple? Dis Colon Rectum 1994; 37(9): 885–9.
Pares D. Pathogenesis and treatment of fistula in ano. Br J Surg 2011; 98(1): 2–3.
Lewis R, Lunniss PJ, Hammond TM. Novel biological strategies in the management of anal fistula. Colorectal Dis 2012; 14(12): 1445–5.
Goffin V, Binart N, Touraine P, Kelly PA. Prolactin: the new
biology of an old hormone. Annu Rev Physiol 2002; 64: 47–67.
Webster Marketon JI, Glaser R. Stress hormones and immune function. Cell Immunol 2008; 252(1–2): 16–26.
De Bellis A, Bizzarro A, Pivonello R, Lombardi G, Bellastella A. Prolactin and autoimmunity. Pituitary 2005; 8(1): 25–30.
Krishnan N, Thellin O, Buckley DJ, Horseman ND, Buckley AR. Prolactin suppresses glucocorticoid-induced thymocyte apop-tosis in vivo. Endocrinology 2003; 144(5): 2102–10.
Xu D, Lin L, Lin X, Huang Z, Lei Z. Immunoregulation of
autocrine prolactin: suppressing the expression of costimulatory molecules and cytokines in T lymphocytes by prolactin
receptor knockdown. Cell Immunol 2010; 263(1): 71–8.
Bouchard B, Ormandy CJ, Di Santo JP, Kelly PA. Immune system development and function in prolactin receptor-deficient mice. J Immunol 1999; 163(2): 576–82.
Celi D, Desogus AI, Cucinotta A, Lucibello L, Giordano T, Metro D, et al. Complex anal fistula with a recess above the levatorani muscles: report of a case complicated by haemorrhagic colitis. Chir Ital 2005; 57(4): 531–4. (Italian)
Yu-Lee LY. Prolactin modulation of immune and inflammato-ry responses. Recent Prog Horm Res 2002; 57: 435–55.
Corbacho AM, Valacchi G, Kubala L, Olano-Martyin E, Schock BC, Kenny TP, et al. Tissue-specific gene expression of prolactin re-ceptor in the acute-phase response induced by lipopolysaccha-rides. Am J Physiol Endocrinol Metab 2004; 287(4): E750–7.
Corbacho AM, Macotela Y, Nava G, Eiserich JP, Cross CE, Martinez de la Escalera G, et al. Cytokine induction of prolactin receptors mediates prolactin inhibition of nitric oxide synthesis in pulmonary fibroblasts. FEBS Lett 2003; 544(1–3): 171–5.
McCann SM, Kimura M, Karanth S, Yu WH, Mastronardi CA,
Rettori V. The mechanism of action of cytokines to control the release of hypothalamic and pituitary hormones in infection. Ann N Y Acad Sci 2000; 917: 4–18.
Bilezikjian LM, Vale WW. The local control of the pituitary by Activin signaling and modulation. Open Neuroendocrinol J 2011; 4: 90–101.
Berczi I, Bertok L, Chow DA. Natural immunity and neuroim-mune host defense. Ann N Y Acad Sci 2000; 917: 248–57.
Buchanan GN, Sibbons P, Osborn M, Bartram CI, Ansari T, Halligan S, et al. Experimental model of fistula-in-ano. Dis Colon Rectum 2005; 48(2): 353–8.
Das R, Vonderhaar BK. Transduction of prolactin’s (PRL) growth signal through both long and short forms of the PRL receptor. Mol Endocrinol 1995; 9(2): 1750–9.
Hu ZZ, Zhuang L, Meng J, Leondires M, Dufau ML. The human prolactin receptor gene structure and alternative promoter uti-lization: the generic promoter hPIII and a novel human pro-moter hP(N). J Clin Endocrinol Metab 1999; 84(3): 1153–6.
