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[Cancer Research 65, 2554-2559, April 1, 2005]
© 2005 American Association for Cancer Research

Priority Reports

PIK3CA Mutations Correlate with Hormone Receptors, Node Metastasis, and ERBB2, and Are Mutually Exclusive with PTEN Loss in Human Breast Carcinoma

Lao H. Saal1,4,6, Karolina Holm6, Matthew Maurer4, Lorenzo Memeo2, Tao Su5, Xiaomei Wang5, Jennifer S. Yu2,4, Per-Olof Malmström6, Mahesh Mansukhani2, Jens Enoksson7, Hanina Hibshoosh2,5, Åke Borg6,8 and Ramon Parsons2,3,4,5

1 Integrated Program in Cellular, Molecular, and Biophysical Studies, Departments of 2 Pathology and 3 Medicine, 4 Institute for Cancer Genetics, 5 Herbert Irving Comprehensive Cancer Center, College of Physicians and Surgeons, Columbia University, New York, New York; Departments of 6 Oncology and 7 Pathology, 8 Lund Strategic Research Center for Stem Cell Biology and Cell Therapy, Lund University, Lund, Sweden

Requests for reprints: Ramon Parsons, Institute for Cancer Genetics, 1150 St. Nicholas Avenue, New York, NY 10032. Phone: 212-851-5278; Fax: 212-851-5256; E-mail: rep15{at}columbia.edu.


   Abstract
Top
 Abstract
Introduction
 Materials and Methods
 Results and Discussion
 References
 
Deregulation of the phosphatidylinositol 3-kinase (PI3K) pathway either through loss of PTEN or mutation of the catalytic subunit {alpha} of PI3K (PIK3CA) occurs frequently in human cancer. We identified PIK3CA mutations in 26% of 342 human breast tumor samples and cell lines at about equal frequency in tumor stages I to IV. To investigate the relationship between PTEN and PIK3CA, we generated a cohort of tumors that had lost PTEN expression and compared it with a matched control set that had retained PTEN. A highly significant association between PIK3CA mutations and retention of PTEN protein expression was observed. In addition, PIK3CA mutations were associated with expression of estrogen and progesterone receptors (ER/PR), lymph node metastasis, and ERBB2 overexpression. The fact that PIK3CA mutations and PTEN loss are nearly mutually exclusive implies that deregulated phosphatidylinositol-3,4,5-triphosphate (PIP3) is critical for tumorigenesis in a significant fraction of breast cancers and that loss of PIP3 homeostasis by abrogation of either PIK3CA or PTEN relieves selective pressure for targeting of the other gene. The correlation of PIK3CA mutation to ER/PR-positive tumors and PTEN loss to ER/PR-negative tumors argues for disparate branches of tumor evolution. Furthermore, the association between ERBB2 overexpression and PIK3CA mutation implies that more than one input activating the PI3K/AKT pathway may be required to overcome intact PTEN. Thus, mutation of PIK3CA is frequent, occurs early in carcinoma development, and has prognostic and therapeutic implications.

Key Words: PTEN • PIK3CA • PI-3 kinase • breast cancer • ERBB2


   Introduction
Top
 Abstract
 Introduction
Materials and Methods
 Results and Discussion
 References
 
Phosphatidylinositol-3,4,5-triphosphate (PIP3) is an important lipid second messenger in tumorigenesis, in particular by activating AKT and other pathways which inhibit apoptosis and promote cellular growth, proliferation, cell motility, angiogenesis, and the accumulation of additional genetic defects. In an elegant "on/off" switch, the phosphatidylinositol 3-kinase (PI3K) holoenzyme, in response to signals transmitted via growth factor receptor tyrosine kinases, phosphorylates phosphatidylinositol-4,5-bisphosphate at the 3'-OH position of the inositol ring to form PIP3, whereas PTEN catalyzes the precise opposite reaction, thereby reducing the pool of PIP3, inhibiting growth signals and suppressing tumor formation (1). The importance of this pathway in cancer is highlighted by the following observations: the PTEN tumor suppressor is inactivated by mutations in a variety of sporadic human tumors and cancer-predisposing hereditary syndromes, epigenetic silencing of PTEN occurs in many forms of cancer, and loss of PTEN stimulates tumor development in mice (reviewed in ref. 2). Moreover, one of the catalytic subunits of PI3K, the p110 catalytic subunit {alpha} (PIK3CA), is a transforming oncogene (3), the 3q26 region where PIK3CA is located is amplified in tumors (4, 5), and recently, the PIK3CA gene was shown to have activating mutations in nine types of cancer (6–8). Interestingly, Bachman et al. reported a 25% PIK3CA mutation rate in breast cancer but did not find any association to clinical markers (8). In the current study, we did a large-scale PIK3CA mutational analysis of 292 primary breast tumors and 50 cell lines, and describe for the first time the significant correlation of PIK3CA mutations to lymph node metastasis, estrogen receptor {alpha} (ER), progesterone receptor (PR), and ERBB2 positivity, and an inverse relationship to functional PTEN.


   Materials and Methods
Top
 Abstract
 Introduction
 Materials and Methods
Results and Discussion
 References
 
Samples. DNA from 133 primary breast tumor biopsies were obtained along with corresponding normal tissue DNA for a subset of the same patients, from the Herbert Irving Comprehensive Cancer Center Tumor Bank at Columbia University, NY, and 162 surgically dissected sporadic primary breast tumor biopsies or tumor cell pellets as well as normal tissues from a subset were obtained from the South Sweden Breast Cancer Group collected at the Lund University Hospital, Lund. All samples were blinded and anonymized and obtained in accordance with Columbia University's Institutional Review Board and Lund University's ethics committee approval, respectively. The Columbia cohort contains tumors of all stages, a mixture of sporadic cases and those with significant family histories, were collected between 1986 and 2003, and had varied clinical therapies. The Swedish cohort are all sporadic stage II tumors, were collected between 1985 and 1994, received adjuvant tamoxifen for 2 years, and predominantly come from a larger series of patients (9). For the Swedish cohort, a selection was made such that approximately one third were PTEN protein negative (PTEN–) tumors, and the remaining two thirds were PTEN protein positive (PTEN+) and roughly matched to the PTEN– cases with respect to node and ER status; five tumors with unknown PTEN status were also included. A panel of 51 well-established breast cancer cell lines (see Supplementary data) were grown and harvested according to recommended protocols.

Immunohistochemical analysis. The Swedish cohort of tumors was evaluated for PTEN protein status by immunohistochemistry (IHC) on 4-µm formalin-fixed, paraffin-embedded tissue sections essentially as previously described (10, 11). Anti-PTEN Ab-2 (Neomarkers, Fremont, CA) was applied at 1:300 dilution. As ERBB2 analysis was not routine at the time of diagnosis for the majority of Swedish cases, a subset of 97 tumors were evaluated for ERBB2 status using the A0485 antibody (DakoCytomation, Glostrup, Denmark) at 1:1,000. All immunohistochemistry was done using the DakoCytomation TechMate 500 Plus staining system using sodium citrate pH 6.0 antigen retrieval buffer, manufacturer's recommended reagents and standard microwave streptavidin immunoperoxidase protocol, with the exception that anti-PTEN antibody was applied for 2 hours. PTEN staining intensity scores for invasive tumor and nonneoplastic cells were recorded by two independent pathologists (J. Enoksson and H. Hibshoosh) essentially as described in ref. (11) with further details in the Supplementary data. ERBB2 membranous staining was scored (H. Hibshoosh) according to the DAKO system scale: 0, 1+, 2+, 3+, with 0/1+ recorded as ERBB2 negative (ERBB2–), and 2+/3+ recorded ERBB2 positive (ERBB2+).

PCR and sequence analysis. Sequencing of PIK3CA exons 1, 2, 4, 5, 7, 9, 12, 13, 18, 20, including intron-exon boundaries was done by PCR amplification and direct sequencing of both strands for all tumors as previously described (6) with some modifications. The Swedish series were also analyzed for mutations in PTEN exons 1 to 9 including intron-exon boundaries. Further details are described in the Supplementary data.

Statistical analysis. The Pearson {chi}2 test was used for correlation analyses with a P < 0.05 used as the cutoff for decisions of statistical significance.


   Results and Discussion
Top
 Abstract
 Introduction
 Materials and Methods
 Results and Discussion
References
 
To ensure a more complete understanding of the PIK3CA mutation spectrum in breast cancer, we did mutational analysis in two large cohorts of breast tumors and a large panel of breast tumor cell lines. All of the 10 exons in which PIK3CA mutations have been previously described were analyzed (6). The Swedish cohort was assembled to specifically address genetic associations to PTEN. To investigate the potential correlations to PIK3CA mutations in a more diverse sampling of breast tumors, the Columbia cohort was obtained. Patient clinical demographics are summarized in Table 1. In addition, 51 well-established breast cancer cell lines were analyzed (Supplementary Table S1). More than 98% of over 7000 sequence reads were of high quality and informative; three tumors and one cell line were excluded due to consistently poor sequence quality. PIK3CA mutations were identified in 77 of 292 (26%) primary breast tumors and 14 of 50 (28%) breast cancer cell lines, similar to the results of Bachman et al., who reported a mutation rate of 22% in a set of 41 breast tumors and 30% among 12 cell lines (8). The PIK3CA mutation frequency in the Columbia set (32 of 131) was similar to the Swedish set (45 of 161), notwithstanding the differences in their selection.


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  		Table 1. Clinical demographics of 292 human breast tumors

 
Mutations clustered in two previously reported "hotspot" regions in exons 9 and 20, corresponding to the accessory (helical) and catalytic domains of PIK3CA, respectively (Figs. 1 and 2B). Expanding upon the observation of Bachman et al., in which three mutations in exon 9 and eight mutations in exon 20 were found among 53 samples (8), we found 31 mutations in exon 9 and 49 mutations in exon 20. This is strong evidence that exon 20 mutations predominate in breast cancer, in contrast to colorectal cancer where exon 9 mutations predominate (6). Whereas mutations in exon 7 (C2 domain) have not been reported in breast cancer owing to small sample size (6) or nonanalysis (8), we found this exon to be a third mutation hotspot with seven mutations. Exons 1, 4, and 13 each had two mutated samples, and we found only one mutation in exon 18. All mutations fall into either the PI3K p85 regulatory subunit binding domain, the C2 domain, the accessory region, or the kinase domain (Fig. 1). The molecular details of how each mutation specifically affects the function and regulation of the kinase requires further study, although the H1047R mutation has been shown to increase its kinase activity (6). Interestingly, two tumors and one cell line contained more than one mutation, each with an exon 20 mutation complemented by a mutation in either exon 7 or 9 (H1047L with E418K, T1025S with E545K, H1047R with P539R, respectively). The significance of these double mutants is unknown, but one may hypothesize that this could indicate a multiclonal tumor, that some mutations are less potent activators of the kinase and that additional mutations to the same allele confer an added growth advantage, or could signify a second hit in the alternate allele. We confirmed the mutational status of all 12 cell lines described by Bachman et al. (8), with the exception of MCF-7 which they report as having E542K, and we found to harbor E545K.



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  		Figure 1. PIK3CA protein and functional domains. The mutations discovered in the present study are graphed with the amino acid substitutions indicated and the frequency of each given within parentheses. Amino acid changes from novel nucleotide mutations (red) and previously documented somatic mutations (black). Nucleotide substitutions in the PIK3CA coding sequence (where 1 is the first base of the start codon) for each mutation is as follows: C178A:Q60K, G333C:K111N, T1035A:N345K, G1252A:E418K, T1258C:C420R, G1357A:E453K, C1616G:P539R, G1624A:E542K, G1633A:E545K, A2102C:H701P, C2727G:F909L, A3073T:T1025S, A3127G:M1043V, T3132A:N1044K, A3140T:H1047L, A3140G:H1047R, C3139T:H1047Y, and G3145C:G1049R. Cell line mutations are presented in Supplementary Table S1. p85, PI3K p85 regulatory subunit binding domain; C2, C2 calcium/lipid-binding region; accessory, PI3K accessory (helical) domain; kinase, PI3/4-kinase domain.

 


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  		Figure 2. A, PTEN immunohistochemical staining. Typical staining results. Left, PTEN+ tumor. Right, PTEN– tumor. Red arrows, tumor cells. Green arrows, PTEN+ normal cells that serve as an internal control. B, PIK3CA mutations. Typical chromatogram traces are shown for exons 9 (left) and 20 (right) with normal wild-type sequence (top) and cancer-derived mutant sequence (bottom). Arrows, position of the missense mutations with nucleotide and amino acid substitutions noted.

 
Nine novel nucleic acid substitutions resulting in missense mutations were discovered in our analysis (Fig. 1). For each mutated tumor sample, corresponding normal tissue DNA, when available, was sequenced to verify that the mutation was somatic. Two novel mutations (E453K and N1044K) and an additional 17 mutated tumors with mutations shown somatic in other studies (6–8) were validated in this manner; the remaining seven novel mutations were cross-referenced and not identified in any normal DNAs in another large study (6).9 Consistent with an oncogenic nature of these mutations, all mutations described in this study were missense, and, except for one mutation in the SUM-185 cell line, seemed heterozygous. Of note, nearly identical sequence to that of PIK3CA exons 9, 12, and 13 and their intron-exon boundaries can also be found at 22q11.2, and therefore care must be taken when designing primers and analyzing data (see Supplementary data).

In the Swedish cohort, PTEN protein expression and mutational status were determined. A larger set of 343 stage II cases (9) were evaluated by immunohistochemistry, of which 55 were scored PTEN negative (PTEN–, little to no tumor staining in relation to normal cells on the same tissue section), and in agreement with the literature (12, 13) PTEN protein expression was significantly correlated to ER and PR positivity (P < 0.0001 and P = 0.001, respectively; data not shown; Fig. 2). From this larger set, 48 of the PTEN– tumors were selected for this study based on availability of snap-frozen tumor biopsies, and roughly matched to 109 PTEN+ (relatively equal tumor PTEN protein levels when compared with internal control normal cells) tumors, with respect to node and ER status where possible; five cases with undetermined PTEN protein status were also selected and subsequently one PTEN– case was excluded due to bad sequence (Table 1). Correlation analysis between PIK3CA mutations to PTEN IHC status revealed a highly significant association, in that the majority of PIK3CA mutations were found in PTEN+ cases (P = 0.0066; Table 2). All nine exons of PTEN were sequenced in these cases and eight mutations were found (5%). This was not surprising, because in sporadic breast cancer PTEN is infrequently altered via mutation (14, 15). Nevertheless, combination of the PTEN mutation data with the PTEN expression data improved the inverse correlation between PIK3CA mutations and abrogated PTEN (PTEN– and PTEN mutants counted together; P = 0.0037; Table 2). Surprisingly, two tumors were double mutants for PIK3CA and PTEN: PIK3CA H701P with a PTEN exon 5 frame-shift truncation mutation, and PIK3CA C420R with a PTEN exon 7 frame-shift truncating mutation. Mutational status of these two cases was rigorously verified (see Supplementary data).


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  		Table 2. PIK3CA correlation analysis

 
The rare overlap between PIK3CA mutations and PTEN inactivation is consistent with the fact that these two proteins catalyze the opposite reaction and may indicate that after activation of PIK3CA or loss of PTEN, either of which results in the net increase of PIP3 and effective oncogenic activation of the pathway, there is reduced selective advantage for the other gene to be also targeted. This observation also reinforces a recent report by Broderick et al. (7), who analyzed high-grade brain tumors and found no PIK3CA mutations in samples harboring PTEN mutations (which is the most common way PTEN is inactivated in those tumor types) among 47 tumors analyzed. In this light, the presence of two PIK3CA/PTEN-double mutants may be an indication that H701P and C420R are less potent activators of the pathway.

We were interested in testing the relationship between PIK3CA mutational status and other known clinicopathologic markers (Table 2). We found PIK3CA mutations to be highly correlated to lymph node involvement (N+), ER positivity (ER+), and PR positivity (PR+; P = 0.0375, P = 0.0001, P = 0.0063, respectively), three clinical markers associated to patient survival and response to therapy (16, 17). This is in contrast to Bachman et al. who found no correlation to ER/PR in their study (8), which may be due to their small sample size compared with the present study. When only analyzing the stage II tumors from both Swedish and Columbia cohorts together, the correlations to node, ER, and PR status improved (P = 0.0239, P < 0.0001, and P = 0.0041, respectively; Table 2). This is not unexpected given the known associations between tumor stage and ER/PR and node status. Moreover, PIK3CA mutations were significantly associated with ERBB2 overexpression (P = 0.0415), another predictive marker in breast cancer (18), and the correlation was more significant when testing only stage II cases (P = 0.0371; Table 2). This result is also in contrast to Bachman et al. who found no correlation to ERBB2 staining (8).

The frequency of PIK3CA mutations in several clinically relevant groups is worth highlighting. Approximately 33% of tumors positive for either ER, PR, node involvement, or ERBB2 harbored PIK3CA mutations (Table 2). Given the strong correlations to individual markers, it is not surprising that the mutation rate increased when we investigated subgroups defined by more than one marker (e.g., to 45% in ER+/ERBB2+ stage II tumors); in contrast, <7% were mutated among ER–/ERBB2– tumors (P = 0.0002, n = 64, data not shown). In both the ER+/ERBB2– and ER–/ERBB2+ subgroups, the mutation frequency was the same as the overall mutation rate (26%) in the complete data set (data not shown). As expected, analyzing further refined subgroups made the differences in mutation rate more extreme: 58% among ER+/ERBB2+/N+ stage II cases versus less than 14% in ER–/ERBB2–/N– (P = 0.0062, n = 34, data not shown). It is also worth noting the distribution of clinical markers among PIK3CA mutants: 95% were PTEN wild type, 86% PTEN+, 78% ER+, 68% N+, 65% PR+, and 48% ERBB2+ (Table 2).

The correlations between PIK3CA mutations and PTEN, ER/PR, node, and ERBB2 status present interesting questions. The observation that ER+/PR+ tumors more often have PIK3CA mutations whereas ER–/PgR– tumors more often have loss of PTEN may reflect differences in pathogenesis and disease progression between hormone receptor positive and negative tumors, thereby defining two separate branches of breast tumor development. Furthermore, our finding that PIK3CA mutations correlate with node metastasis and a report showing PTEN loss also associated with node metastasis (13) suggest that increased PIP3 production and activation of the PI3K/AKT pathway may enhance invasion of cancer cells to lymph nodes. This last postulation is corroborated by the findings that PTEN inhibits cell migration (19), and that PIP3 regulates cell motility (20). Lastly, our result that PIK3CA mutations correlate to ERBB2 overexpression argues that multiple positive inputs on the pathway may be needed to overcome intact PTEN (notably, both PIK3CA/PTEN-double mutants are ERBB2–). This is clinically significant as intact PTEN is required for therapeutic response to Herceptin (21). Identification of the tumors that are ER+/ERBB2+ and PIK3CA mutation positive, a group likely to have normal PTEN, and treatment with a combination of drugs against the ER, ERBB2, and PIK3CA pathways is a therapeutic approach that should be explored.

Given the significant association of PIK3CA mutations to four clinical markers with varied prognostic implications, ER+ and PR+ (good prognosis), and N+ and ERBB2+ (bad prognosis), we did survival analyses. No significant associations were found between PIK3CA mutational status and distant disease-free survival, recurrence-free survival, or overall survival within all tumors, or when stratified by cohort, stage, lymph node, or ER status (data not shown). It is possible that the association of PIK3CA mutations to good and bad prognostic markers dilutes its association to outcome. Moreover, our selection of tumors was not ideal for survival analysis, as the Swedish set were matched on node and ER status, the Columbia cohort had varied clinical therapies and the duration of follow-up may not have been long enough (Table 1). PIK3CA mutations were not associated with tumor size, stage, ploidy, or S-phase fraction (data not shown).

In conclusion, in our study of PIK3CA mutations in a large set of breast cancers and breast cancer cell lines, we uncovered a mutation rate of 26%. We found PIK3CA mutations in all stages of breast cancer, indicating that mutations are an early event in carcinoma development. To determine the relationship between PIK3CA mutational status and PTEN function, we analyzed a subset of our primary tumors for the expression of PTEN protein and for the presence of PTEN mutations. We report that PIK3CA tumor mutations correlate to intact PTEN, lymph node metastasis, and expression of ER, PR, and ERBB2. We did not find any association with survival, although further study of material better suited for such analysis is warranted and is currently under way. We provide evidence for two separate paths for breast tumor development: hormone receptor positive with PIK3CA mutations and hormone receptor negative with PTEN loss. Taken together with the observation that 15% to 35% of breast cancers have loss of PTEN expression, our data would suggest that at least half of all breast cancers have deregulated production of PIP3. When including aberrations in other upstream and downstream members of the pathway, such as ERBB2 and AKT, it would seem that the majority of breast tumors have activation of the pathway, making this pathway an attractive target for pharmacologic interventions and highlighting the importance of molecular profiling for personalized medicine. In particular, directed small molecule antagonism of PIK3CA proteins may be an effective measure for the treatment of breast cancer, regardless of whether it has a PIK3CA mutation or a loss of PTEN protein expression. It is interesting to note that many forms of human cancer have high frequency inactivation of PTEN and activation of PIK3CA. Given that alterations of these two genes tend to be mutually exclusive, it is likely that a very substantial proportion of most common malignancies such as carcinomas of the breast, lung, colon, and prostate have selected for activation of the PI3K pathway.

Note added in proof. Since we submitted this report, Campbell et al. have published a PIK3CA mutational study including 70 primary breast tumors but found no association to histologic subtype, grade, ER or node status (22).


   Acknowledgments
 
Grant support: NIH, Medical Scientist Training grants 5T32 GM07367-29 (L. Saal and J. Yu) and CA082783 and CA097403 (R. Parsons), Avon Foundation (H. Hibshoosh and R. Parsons), Swedish Cancer Society (Å. Borg), Berta Kamprad Foundation (Å. Borg), Gunnar Nilsson Cancer Foundation (Å. Borg), Lund University Hospital Foundations (Å. Borg), King Gustav V:s Jubilee Foundation (Å. Borg), and Ingabritt and Arne Lundberg Foundation (Å. Borg).

The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked advertisement in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

We thank the participating departments of the South Sweden Breast Cancer Group for providing samples; Vladan Miljkovic, Kristina Lövgren, Eva Rambech, and Carina Strand for expert technical assistance; John Jakob for tissue culture work; Ita Horan and Linda Lowenstein for administrative services; Susan Kistler for data retrieval assistance; and Sofia Gruvberger-Saal for helpful discussions.


   Footnotes
 
Note: L.H. Saal and K. Holm contributed equally to this study.

Å. Borg and R. Parsons share senior authorship.

Supplementary data for this article are available at Cancer Research Online (http://cancerres.aacrjournals.org).

9 Y. Samuels, personal communication. Back

Received 11/ 1/04. Revised 12/17/04. Accepted 12/30/04.


   References
Top
 Abstract
 Introduction
 Materials and Methods
 Results and Discussion
 References
 

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ASCO Educational Book, January 1, 2008; 2008(1): 120 - 126.
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C.-H. Huang, D. Mandelker, O. Schmidt-Kittler, Y. Samuels, V. E. Velculescu, K. W. Kinzler, B. Vogelstein, S. B. Gabelli, and L. M. Amzel
The Structure of a Human p110{alpha}/p85{alpha} Complex Elucidates the Effects of Oncogenic PI3K{alpha} Mutations
Science, December 14, 2007; 318(5857): 1744 - 1748.
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A. Andres-Pons, I. Rodriguez-Escudero, A. Gil, A. Blanco, A. Vega, M. Molina, R. Pulido, and V. J. Cid
In vivo Functional Analysis of the Counterbalance of Hyperactive Phosphatidylinositol 3-Kinase p110 Catalytic Oncoproteins by the Tumor Suppressor PTEN
Cancer Res., October 15, 2007; 67(20): 9731 - 9739.
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P. Angelo, M. Anita, A. Amalia, and T. Stefania
Phosphatidylinositol 3-Kinase in Breast Cancer: Where from Here?
Clin. Cancer Res., October 15, 2007; 13(20): 5988 - 5990.
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M. Barbareschi, F. Buttitta, L. Felicioni, S. Cotrupi, F. Barassi, M. Del Grammastro, A. Ferro, P. Dalla Palma, E. Galligioni, and A. Marchetti
Different Prognostic Roles of Mutations in the Helical and Kinase Domains of the PIK3CA Gene in Breast Carcinomas
Clin. Cancer Res., October 15, 2007; 13(20): 6064 - 6069.
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M. J. Ellis and R. Crowder
"PIKing" the Winner for Phosphatidylinositol 3-Kinase Inhibitors in ErbB2-Positive Breast Cancer: Let's Not "PTENed" It's Easy!
Clin. Cancer Res., October 1, 2007; 13(19): 5661 - 5662.
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E. Hirsch, C. Costa, and E. Ciraolo
Phosphoinositide 3-kinases as a common platform for multi-hormone signaling
J. Endocrinol., August 1, 2007; 194(2): 243 - 256.
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N. Miled, Y. Yan, W.-C. Hon, O. Perisic, M. Zvelebil, Y. Inbar, D. Schneidman-Duhovny, H. J. Wolfson, J. M. Backer, and R. L. Williams
Mechanism of Two Classes of Cancer Mutations in the Phosphoinositide 3-Kinase Catalytic Subunit
Science, July 13, 2007; 317(5835): 239 - 242.
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G. Perez-Tenorio, L. Alkhori, B. Olsson, M. A. Waltersson, B. Nordenskjold, L. E. Rutqvist, L. Skoog, and O. Stal
PIK3CA Mutations and PTEN Loss Correlate with Similar Prognostic Factors and Are Not Mutually Exclusive in Breast Cancer
Clin. Cancer Res., June 15, 2007; 13(12): 3577 - 3584.
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M. Dimri, M. Naramura, L. Duan, J. Chen, C. Ortega-Cava, G. Chen, R. Goswami, N. Fernandes, Q. Gao, G. P. Dimri, et al.
Modeling Breast Cancer-Associated c-Src and EGFR Overexpression in Human MECs: c-Src and EGFR Cooperatively Promote Aberrant Three-dimensional Acinar Structure and Invasive Behavior
Cancer Res., May 1, 2007; 67(9): 4164 - 4172.
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L. H. Saal, P. Johansson, K. Holm, S. K. Gruvberger-Saal, Q.-B. She, M. Maurer, S. Koujak, A. A. Ferrando, P. Malmstrom, L. Memeo, et al.
Poor prognosis in carcinoma is associated with a gene expression signature of aberrant PTEN tumor suppressor pathway activity
PNAS, May 1, 2007; 104(18): 7564 - 7569.
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M. Gymnopoulos, M.-A. Elsliger, and P. K. Vogt
Rare cancer-specific mutations in PIK3CA show gain of function
PNAS, March 27, 2007; 104(13): 5569 - 5574.
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 CarcinogenesisHome page
C. Blanco-Aparicio, L. Perez-Gallego, B. Pequeno, J. F.M. Leal, O. Renner, and A. Carnero
Mice expressing myrAKT1 in the mammary gland develop carcinogen-induced ER-positive mammary tumors that mimic human breast cancer
Carcinogenesis, March 1, 2007; 28(3): 584 - 594.
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A. Hollestelle, F. Elstrodt, J. H.A. Nagel, W. W. Kallemeijn, and M. Schutte
Phosphatidylinositol-3-OH Kinase or RAS Pathway Mutations in Human Breast Cancer Cell Lines
Mol. Cancer Res., February 1, 2007; 5(2): 195 - 201.
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J.-S. Kim, C. Lee, C. L. Bonifant, H. Ressom, and T. Waldman
Activation of p53-Dependent Growth Suppression in Human Cells by Mutations in PTEN or PIK3CA
Mol. Cell. Biol., January 15, 2007; 27(2): 662 - 677.
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N. Maruyama, Y. Miyoshi, T. Taguchi, Y. Tamaki, M. Monden, and S. Noguchi
Clinicopathologic Analysis of Breast Cancers with PIK3CA Mutations in Japanese Women
Clin. Cancer Res., January 15, 2007; 13(2): 408 - 414.
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S. Uddin, A. R. Hussain, A. K. Siraj, P. S. Manogaran, N. A. Al-Jomah, A. Moorji, V. Atizado, F. Al-Dayel, A. Belgaumi, H. El-Solh, et al.
Role of phosphatidylinositol 3'-kinase/AKT pathway in diffuse large B-cell lymphoma survival
Blood, December 15, 2006; 108(13): 4178 - 4186.
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G. L. Gallia, V. Rand, I-M. Siu, C. G. Eberhart, C. D. James, S. K.N. Marie, S. M. Oba-Shinjo, C. G. Carlotti, O. L. Caballero, A. J.G. Simpson, et al.
PIK3CA Gene Mutations in Pediatric and Adult Glioblastoma Multiforme
Mol. Cancer Res., October 1, 2006; 4(10): 709 - 714.
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J. W. Watters and C. J. Roberts
Developing gene expression signatures of pathway deregulation in tumors.
Mol. Cancer Ther., October 1, 2006; 5(10): 2444 - 2449.
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A. Vilgelm, Z. Lian, H. Wang, S. L. Beauparlant, A. Klein-Szanto, L. H. Ellenson, and A. Di Cristofano
Akt-Mediated Phosphorylation and Activation of Estrogen Receptor {alpha} Is Required for Endometrial Neoplastic Transformation in Pten+/- Mice.
Cancer Res., April 1, 2006; 66(7): 3375 - 3380.
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W. Qiu, F. Schonleben, X. Li, D. J. Ho, L. G. Close, S. Manolidis, B. P. Bennett, and G. H. Su
PIK3CA Mutations in Head and Neck Squamous Cell Carcinoma
Clin. Cancer Res., March 1, 2006; 12(5): 1441 - 1446.
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A. G. Bader, S. Kang, and P. K. Vogt
Cancer-specific mutations in PIK3CA are oncogenic in vivo
PNAS, January 31, 2006; 103(5): 1475 - 1479.
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K. Oda, D. Stokoe, Y. Taketani, and F. McCormick
High Frequency of Coexistent Mutations of PIK3CA and PTEN Genes in Endometrial Carcinoma
Cancer Res., December 1, 2005; 65(23): 10669 - 10673.
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S. J. Isakoff, J. A. Engelman, H. Y. Irie, J. Luo, S. M. Brachmann, R. V. Pearline, L. C. Cantley, and J. S. Brugge
Breast Cancer-Associated PIK3CA Mutations Are Oncogenic in Mammary Epithelial Cells
Cancer Res., December 1, 2005; 65(23): 10992 - 11000.
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M. Frattini, S. Signoroni, S. Pilotti, L. Bertario, S. Benvenuti, C. Zanon, A. Bardelli, and M. A. Pierotti
Phosphatase Protein Homologue to Tensin Expression and Phosphatidylinositol-3 Phosphate Kinase Mutations in Colorectal Cancer
Cancer Res., December 1, 2005; 65(23): 11227 - 11227.
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G. Garcia-Rostan, A. M. Costa, I. Pereira-Castro, G. Salvatore, R. Hernandez, M. J.A. Hermsem, A. Herrero, A. Fusco, J. Cameselle-Teijeiro, and M. Santoro
Mutation of the PIK3CA Gene in Anaplastic Thyroid Cancer
Cancer Res., November 15, 2005; 65(22): 10199 - 10207.
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